• 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
-
11 to 20 of 500 Results *
 < 
 1 
 2 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
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]
qfix radiotherapy chair WFR/AQUAPLAST CORP. k120916 06/20/2012
clinical chloride analyzer, chloride test system, sweat chloride analyzer, chloridometer, chloride coulometric WESCOR, INC. k121823 03/27/2013
iexaminer system with panoptic plus Welch Allyn, Inc. k223381 03/15/2023
milestone spinal system WEIGAO ORTHOPAEDIC DEVICE CO., LTD k133053 07/15/2014
60cc irrigating syringe, piston type, WAZ INDUSTRIES, INC. k791998 10/26/1979
uropower W.O.M. WORLD OF MEDICINE AG k022721 08/26/2003
cold/hot pack W.G. WHITNEY CORP. k803299 01/15/1981
nutrisafe 2 VYGON CORP. k060944 09/15/2006
vycor medical viewsite brain access system (“vbas”) and vbas with alignment clip (“vbas ac”) (together the “vbas family”) Vycor Medical INC. k202694 01/14/2021
peep/cpap valve VICKERS AMERICA MEDICAL CORP. k781332 10/04/1978

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