• 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
-
131 to 140 of 500 Results *
Decision Date To: 07/22/2019
 < 
 9 
 10 
 11 
 12 
 13 
 14 
 15 
 16 
 17 
 18 
 > 
Results per Page
New Search  
Export all 500 Records to ExcelExport to Excel | Download Files | More About 510(k)
Device Name
Sort by Device Name [A-Z]
Sort by Device Name [Z-A]
Applicant
Sort by Applicant [A-Z]
Sort by Applicant [Z-A]
510(K)
Number
Sort by 510(k) Number [0-9]
Sort by 510(k) Number [9-0]
Decision
Date
Sort by Decision Date [0-9]
Sort by Decision Date [9-0]
computed radiography scanner 3DISC AMERICAS K133106 01/15/2014
quantorview 3DISC AMERICAS K151687 08/03/2015
3dfis, model ies-fl-101 3DSHARP, INC. K013841 01/17/2002
procedure rehearsal studio 3DSYSTEMS, SIMBIONIX PRODUCTS K153705 09/02/2016
sonalis, model 2000 3G ULTRASOUND, INC. K043189 02/09/2005
cryonize tm 3JT ENTERPRISES LLC K103310 02/09/2011
3l surgical drapes 3L MEDICAL PRODUCTS CO., LTD. K043015 08/15/2005
3mtm attesttm mini auto-reader 490m 3M K200092 04/15/2020
avi micro 285cm infusion pump 3M AVI, INC. K903788 09/04/1990
avi micro 845 dual channel infusion pump 3M AVI, INC. K903786 09/05/1990

*   The maximium 500 devices meeting your search criteria returned. Please narrow your search.
-
-