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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, donor, cmv
510(k) Number BK950046
Tradename Abbott CMV Total AB EIA
Device Name Test, Donor, CMV
Classification Product Code
MZE  
Date Received08/23/1995
Decision Date 12/22/1995
Decision substantially equivalent (SE)
Review Advisory Committee Immunology
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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