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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name kit, quality control for blood banking reagents
510(k) Number BK080027
Tradename ALBAcheck - BGS Reagent Control for Anti-D
Device Name Kit, Quality Control for Blood Banking Reagents
Regulation Number864.9650
Classification Product Code
KSF  
Date Received06/09/2008
Decision Date 07/29/2008
Decision substantially equivalent (SE)
Classification Advisory Committee Hematology
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 Yes
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