• 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
-
1 to 10 of 61 Results
ProductCode: NBW Decision Date From: 01/01/2012 Decision Date To: 12/31/2012
 
 1 
 2 
 3 
 4 
 5 
 6 
 7 
 > 
Results per Page
New Search  
Export all 61 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]
glooko logbook charts GLOOKO, INC. K122142 12/21/2012
nova one blood glucose monitor NOVA BIOMEDICAL CORPORATION K122435 12/20/2012
on call vivid blood glucose monitoring system ACON LABORATORIES, INC. K123010 12/14/2012
da01 blood glucose monitoring system DELBIO INCORPORATION K120866 12/11/2012
blood glucose monitoring system ANDON MEDICAL CO., LTD K120813 12/07/2012
omnipod insulin managment system INSULET CORPORATION K122953 12/07/2012
genstrip test strip model 100-201 SHASTA TECHNOLOGIES, LLC K103542 11/30/2012
acon on call vivid pal blood glucose monitoring system ACON LABORATORIES, INC. K122110 11/21/2012
accu-chek inform ii blood glucose monitoring system Roche Diagnostics K121679 10/11/2012
genesis health technologies blood glucose monitoring system TaiDoc Technology Corporation K121224 09/19/2012
-
-