• 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 5 of 5 Results
ProductCode: FPA Applicant: NIPRO MEDICAL CORP Decision Date To: 08/28/2014
Results per Page
New Search
Export all 5 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]
nipro huber infusion set, excel huber in nipro medical corporation K113471 10/18/2012
nipro safe touch huber infusion set nipro medical corporation K113470 10/17/2012
nipro safetouch huber infustion set nipro medical corp. K081210 10/21/2008
nipro disposable solution infusion set nipro medical corp. K972493 09/18/1997
nipro disposable solution infusion set nipro medical corp. K970076 03/27/1997
-
-