• 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 microfilter, blood transfusion
510(k) Number BK050041
Tradename Leucolab LCG2 Leukoreduction System for Red Blood Cells
Device Name Microfilter, Blood Transfusion
Original Applicant
MacoProductions S.A.S.
3075 breckinridge blvd.
suite 405
duluth,  GA  30096
Regulation Number880.5440
Classification Product Code
CAK  
Date Received07/25/2005
Decision Date 10/12/2005
Decision substantially equivalent (SE)
Classification Advisory Committee General Hospital
Review Advisory Committee General Hospital
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
-
-