• 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
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Biologics Clearance Letters and 510(k) Summaries Back To Search Results
Device Classification Name separator, semi-automated, blood component
510(k) Number BK080010
Tradename The Atreus Whole Blood Processing System
Device Name Semi-automated Blood Component Separator
Original Applicant
Terumo BCT, Inc
10811 w. collins ave.
lakewood,  CO  80215 4498
Classification Product Code
MYY  
Date Received03/13/2008
Decision Date 06/27/2008
Decision substantially equivalent (SE)
Review Advisory Committee Hematology
Type 510(k) Traditional
Total Product Life Cycle (TPLC) TPLC Device Report
Reviewed by Third Party No
Expedited Review No
Combination Product No
In Vitro Product No
-
-