• 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 7 of 7 Results
ProductCode: CAC Applicant: COBE CARDIOVASCULAR, INC. Decision Date To: 05/23/2024
Results per Page
New Search  
Export all 7 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 brat 2 autologous blood salvage system with the crit-line hematocrit sampling system option COBE CARDIOVASCULAR, INC. K991986 09/09/1999
cobe brat 2 system with modified standard volume processing set COBE CARDIOVASCULAR, INC. K974897 03/31/1998
standard volume processing set for the cobe brat 2 autologous blood salvage system COBE CARDIOVASCULAR, INC. K973627 11/03/1997
cobe brat 2 autologous blood salvage system with modified plasma recovery program (prp) COBE CARDIOVASCULAR, INC. K962689 01/28/1997
plasma recovery program for the cobe brat 2 autologous blood salvage system COBE CARDIOVASCULAR, INC. K933960 06/10/1994
brat 2 autologus blood salvage system COBE CARDIOVASCULAR, INC. K933625 12/29/1993
cobe brat systems without reinfusion protection COBE CARDIOVASCULAR, INC. K913773 01/27/1992
-
-