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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name separator, automated, blood cell, diagnostic
510(k) Number BK080048
Tradename AMICUS Separator
Device Name Automated Blood Cell Separators
Original Applicant
Fenwal Inc
three corporate drive
2nd floor
lake zurich,  IL  60047
Regulation Number864.9245
Classification Product Code
GKT  
Date Received09/09/2008
Decision Date 10/02/2008
Decision substantially equivalent (SE)
Classification Advisory Committee Hematology
Review Advisory Committee Hematology
Type 510(k) Special
Total Product Life Cycle (TPLC) TPLC Device Report
Reviewed by Third Party No
Expedited Review No
Combination Product No
In Vitro Product No
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