• 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
-
321 to 330 of 500 Results *
 < 
 32 
 33 
 34 
 35 
 36 
 37 
 38 
 39 
 40 
 41 
 > 
results per page
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]
free testosterone enzymeimmunoassay (eia) kit DIAGNOSTICS BIOCHEM CANADA, INC. k030730 08/18/2003
trimed radial bullet TRI-MED, INC. k030877 02/05/2004
ranfac goldenberg snarecoil soft tissue biopsy (gss) needle RANFAC CORP. k031344 05/23/2003
bifurcated allergy skin testing needle PRECISION MEDICAL PRODUCTS, INC. k031630 08/07/2003
vinyl exam gloves, powder-free, yellow SHANGHAI JIAWANG INDUSTRIAL CO. LTD. k031854 07/25/2003
interpore cross cement restrictor INTERPORE CROSS INTL. k032095 08/08/2003
modification to multitrans culture collection and transport system STARPLEX SCIENTIFIC, INC. k032246 08/13/2003
modificarion to wackers-liu cq software ECLIPSE SYSTEMS, INC. k032500 08/25/2003
biosign steam-24 biological indicator GETINGE USA, INC k032723 10/01/2003
jms blood tubing sets JMS NORTH AMERICA CORP. k032975 08/16/2004

*   The maximum 500 records meeting your search criteria returned. Please narrow your search.
-
-