BNET Business Dictionary

Business Definition for: Premarket

  • used to describe transactions between market members conducted prior to the official opening of the market.
  • Also known as Pretrading

Additional Resources

Premarket notification program on new dietary ingredients.(Noted In The Federal Register)
PREMARKET NOTIFICATION PROGRAM ON NEW DIETARY INGREDIENTS: FDA is soliciting comments on FDA's premarket notification program for new dietary ingredients NDIs. FDA is soliciting comments from industry, consumers and other interested members of the PREMARKET NOTIFICATION PROGRAM ON NEW DIETARY INGREDIENTS: FDA is soliciting...
Tags: FDA
Research articles 2004-10-25
Pyrolytic carbon heart valve receives premarket approval.
Medical Carbon Research Institute MCRI, has announced that the U.S. Food and Drug Administration FDA has issued a premarket approval PMA for the On-X pyrolytic carbon aortic valve. With the PMA, the On-X aortic valve is now available in the Uni Medical Carbon Research Institute MCRI,...
Tags: carbon, FDA
Research articles 2001-09-01
Base Ten submits 510 Premarket Notifications to the FDA for uPACS; ultrasound image archiving system planned for sale in the United States - k
TRENTON, N.J.--BUSINESS WIRE--March 26, 1996--Base Ten Systems Inc. (NASDAQ:NMS-BASEA) announced today that 510k Premarket Notifications for two uPACSTM Picture Archiving System products were submitted to the FDA under the 510k premarket notification process.
Tags: FDA
Research articles 1996-03-26
Group aims to re-energize HP premarket (Furniture Today)
High Point-- While a smaller contingent of retailers than at past events wandered High Point's quiet showroom district last week, be forewarned: reports of premarket's demise may be premature. High Point-- While a smaller contingent of retailers than at past events wandered High Point's quiet...
Tags: Hewlett-Packard Co.
Research articles 2007-03-05
Sunquest Submits 510 Premarket Notification for Transfusion Management Solution
TUCSON, Ariz. -- Sunquest Information Systems, Inc., a market leader in laboratory information systems, today announced that it has provided its 510k Premarket Notification submission to the Food and Drug Administration FDA for the Sunquest Transfusion Manager software application and information system. Before a Class II product can be sold...
Tags: FDA
Research articles 2008-06-10
Premarket approval application for Norian SRS accepted for filing by FDA
CUPERTINO, Calif..--BW HealthWire--April 14, 1997--Norian Corporation of Cupertino, has submitted a Premarket Approval Application PMA to the Food & Drug Administration for an orthopaedic application of its product, Norian SRS Skeletal Repair System.
Tags: FDA
Research articles 1997-04-14
Base Ten's Premarket Approval application to be reviewed by FDA panel on March 31, 1995
TRENTON, N.J.--BUSINESS WIRE--March 6, 1995--Base Ten Systems Inc. (NASDAQ NMS: BASEA) announced today that the company's Premarket Approval PMA application for PRENVALTM I will be reviewed by the FDA's Immunology Advisory Panel on March 31, 1995. PRENVALTM I is the company's first software program designed to meet the new FDA...
Tags: FDA
Research articles 1995-03-06
Corgenix Submits FDA Premarket Notification of AspirinWorks® Test Kit; New Diagnostic Product to Be Used in Assessing Aspirin Effectiveness
DENVER -- Corgenix Medical Corporation (OTC BB: CONX), a worldwide developer and marketer of diagnostic test kits, has submitted a Premarket Notification (510k) to the U.S. Food and Drug Administration FDA for the Company's AspirinWorksR Test Kit, the Company's newest diagnostic product for cardiovascular disease.
Tags: FDA
Research articles 2006-07-20
Base Ten receives two 510 Premarket Notification clearances from FDA
TRENTON, N.J.--BUSINESS WIRE--Aug. 13, 1996--Base Ten Systems Inc. (NASDAQ-NMS: BASEA), announced today that it has received two 510k Premarket Notification clearances from the FDA for its uPACSTM system for archiving ultrasound images.The uPACSTM system digitizes, records, and stores ultrasound images on CD-ROMs as a cost-effective alternative to existing film and...
Tags: Business Wire, clearance, FDA, Government, SOFTWARE
Research articles 1996-08-13
SpectraSCIENCE receives 510 premarket notification clearance from United States Food and Drug Administration for fiberoptic Biopsy Forceps
MINNEAPOLIS--BUSINESS WIRE--Dec. 16, 1996--SpectraSCIENCE, Inc. (NASDAQ: SPSI) announced today that the company has been notified by the United States Food and Drug Administration that it has received 510k premarket notification clearance for its fiberoptic Biopsy Forceps. The SpectraSCIENCE Biopsy Forceps is designed specifically to collect...
Tags: Business Wire, FDA, Government, Minneapolis, PRODUCTIVITY, SpectraScience Inc.
Research articles 1996-12-16
AFTER POLLING DEALERS, BROYHILL LEAVING HIGH POINT PREMARKET.(Broyhill Furniture Industries Inc. not to participate in coming trade show)(Brief Article)
Byline: Cheminne Taylor-Smith HIGH POINT, N.C.-With a hectic market schedule made worse with the addition of the Las Vegas Market, and questions looming about where buyers will actually shop, at least one manufacturer has decided to drop a show. ...
Tags: Broyhill Inc.
Research articles 2005-08-22
StockGuru Price and Volume Alerts for Tuesday July 25, 2006 - One Company Submits FDA Premarket Notification While Another has Joint Venture in India.
M2 PRESSWIRE-25 July 2006-Stockguru.com: StockGuru Price and Volume Alerts for Tuesday July 25, 2006 - One Company Submits FDA Premarket Notification While Another has Joint Venture in IndiaC1994-2006 M2 COMMUNICATIONS LTD RDATE:25072006 Dallas, Texas - StockGuru Price and Volume Alerts for...
Tags: Price and Co.
Research articles 2006-07-25
AngioScore Receives Premarket Approval for AngioSculpt® Scoring Balloon Catheter
Company's Flagship Device Approved for Use in Coronary Artery Disease FREMONT, Calif. -- AngioScore, Inc, a developer of novel angioplasty catheters for use in the treatment of cardiovascular disease, announced today that its flagship product, the AngioSculpt[R] Scoring Balloon Catheter, has received Premarket Approval PMA from the U.S. Food...
Tags: AngioScore Inc.
Research articles 2007-01-09
Novoste Submits Premarket Approval Application To FDA for Beta-Cath System
Business Editors & Health/Medical Writers NORCROSS, Ga.--BW HealthWire--April 17, 2000 Novoste Corporation (Nasdaq: NOVT) announced today that it has submitted a Premarket Approval PMA application to the U.S. Food and Drug Administration for its Beta-CathTM System. Novoste is the first company to submit a PMA application for an...
Tags: Novoste Corp.
Research articles 2000-04-17
Caterpillar, Apple Profits Push Futures Higher
NEW YORK (Reuters) - U.S. stock index futures rose on Tuesday after strong quarterly results from bellwethers Apple and Caterpillar pointed to a solid earnings season. Apple Inc's AAPL profits and sales streaked past Wall Street forecasts on Monday as sales of iPhones and Mac personal computers hit quarterly records,...
Tags: Apple Inc., Earnings, Caterpillar Inc.
News items 2009-10-20
Buffett Buying Burlington Northern in $34 Billion Deal
By Nick Zieminski NEW YORK (Reuters) - Warren Buffett's Berkshire Hathaway Inc will pay $26 billion to buy out railroad Burlington Northern Santa Fe Corp in what the billionaire investor called a bet on the U.S. economy. The deal, Buffett's biggest-ever acquisition, is priced at a premium of 31.5 percent...
Tags: Berkshire Hathaway Inc., Warren Buffett
News items 2009-11-03
Biotech foods must now get FDA clearance before going to market
Concurrently with releasing the draft guidance for voluntary labeling of biotech foods see article above, the Food and Drug Administration FDA is proposing a new rule that will require food producers to notify FDA prior to marketing a food derived from biotechnology. The proposal converts the current voluntary premarket notification...
Tags: biotechnology, FDA, food
Research articles 2001-03-01
UroMed Corporation Announces 510k Submission for Brachytherapy Seeds
NEEDHAM, Mass--BW HealthWire--June 24, 1998--UroMed Corporation (NASDAQ:URMD) announced today that it has submitted a premarket notification 510k application to the U.S. Food and Drug Administration FDA for market clearance in the U.S. for its radioactive seeds to be used to treat prostate cancer. Review times at the FDA are...
Tags: FDA
Research articles 1998-06-24
InnerDyne Receives FDA Clearance to Market Step Product Line With Enhanced Safety and Performance Claims
SUNNYVALE, Calif.--BW HealthWire--Jan. 13, 1999--InnerDyne, Inc. (NASDAQ NM: IDYN) today reported the acceptance by the U.S. Food & Drug Administration FDA of the company's 510k premarket notification based on the demonstrated safety and clinical performance of the StepTM line of minimally invasive surgical access devices and based on InnerDyne's proprietary...
Tags: FDA, performance
Research articles 1999-01-13
FOOD CONTACT NOTIFICATION.(FDA amends regulations)(Brief Article)
FOOD CONTACT NOTIFICATION: The Food and Drug Administration amended the food additive regulations regarding the premarket notification process for food contact substances FCS, which is the primary method for authorizing new uses of food additives t FOOD CONTACT NOTIFICATION: The Food and Drug Administration amended ...
Tags: FDA, food
Research articles 2002-05-27
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