• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

510(K) Premarket Notification

  • Print
  • Share
  • E-mail
-
51 to 60 of 493 Results
 < 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 14 
 > 
 
New Searchexport reports to excelExport to Excel | HelpHelp
Device Name
Sort by Device Name [A-Z]
Sort by Device Name [Z-A]
Applicant
Sort by PMA Number [0-9]
Sort by PMA Number [9-0]
510(K)
Number
Sort by Decision Date [0-9]
Sort by Decision Date [9-0]
Decision
Date
Sort by Decision Date [0-9]
Sort by Decision Date [9-0]
barcomed 5mp2 BARCO NV k000016 03/14/2000
bayer rapidpoint 400 system BAYER CORP. k002738 12/19/2000
bd eclipse hypodermic needle BD MEDICAL SYSTEMS k010188 03/01/2001
bio-absorbable corkscrew model ar-1920b ARTHREX, INC. k003227 01/08/2001
bio-rad %cdt tia AXIS-SHIELD BIOCHEMICALS, ASA k001651 11/22/2000
biomet external wrist plate BIOMET, INC. k003240 12/29/2000
biomet's minimally constrained elbow BIOMET, INC. k003253 01/12/2001
biopatch antimicrobial dressing INTEGRA LIFESCIENCES CORP. k003229 10/26/2001
biosafe capillary blood transport system for testing thyroid stimulating hormone (tsh) BIOSAFE LABORATORIES, INC. k003752 03/23/2001
biosoft resin BIOSOFT INTERNATIONAL CORP. k001640 06/23/2000

-
-