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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name container, empty, for collection & processing of blood & blood components
510(k) Number BK920002
Tradename Ethox Transfer Pack
Device Name Container, Empty, For the Collection '& Processing of Blood/Blood Components
Original Applicant
Ethox Corp.
251 seneca st,
buffalo,  NY  14204
Regulation Number864.9100
Classification Product Code
KSR  
Date Received01/06/1992
Decision Date 09/17/1992
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 No
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