• 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 2 of 2 Results
ProductCode: DWF Applicant: COBE LABORATORIES, INC Decision Date To: 10/25/2014
Results per Page
New Search
Export all 2 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]
cobe heart/lung perfusion and cardiopleg cobe laboratories, inc. K881330 06/10/1988
tubing sets cobe laboratories, inc. K771692 10/04/1977
-
-