Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • 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
-
41 to 50 of 500 Results *
 < 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 > 
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]
wildcat 5f guidewire support catheter, mode w500 AVINGER, INC. k101647 08/06/2010
architect active b-12 (holotranscobalamin) AXIS-SHIELD DIAGNOSTICS, LTD. k112443 12/19/2011
emerg. oxygen kit #65350 & #65399 case B & F MEDICAL PRODUCTS, INC. k802644 12/22/1980
sterican cannula B. BRAUN MEDICAL, INC. k131842 08/20/2013
baumer locking nail BAUMER S.A. k011504 08/14/2001
abt12 multi-purpose solution Bausch & Lomb Incorporated k202932 05/28/2021
bpz02 multipurpose solution BAUSCH & LOMB, INC. k083757 11/18/2009
bausch + lomb (kalifilcon a) soft contact lens, bausch + lomb (kalifilcon a) soft contact lens for astigmatism Bausch + Lomb, Incorporated k200528 06/02/2020
rapid-fill tubeset, model 90005 BAXA CORP. k022523 08/12/2002
bd single lumen needle, syringe and blood collection set BD k021475 07/19/2002

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