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U.S. Department of Health and Human Services

510(k) Premarket Notification
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New Search Biologics Clearance Letters and 510(k) Summaries Back To Search Results
Device Classification Name test, qualitative, for hla, non-diagnostic
510(k) Number BK160017
Tradename HLA Fusion
Device Name Test, Qualitative, for HLA, Non-Diagnostic
Original Applicant
One Lambda, Inc.
21001 kittridge st.
canoga park,  CA  91303
Classification Product Code
MZI  
Date Received03/02/2016
Decision Date 03/08/2017
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 Yes
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