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FDA 510(k) Application Details - K082082
Device Classification Name
Reservoir, Blood, Cardiopulmonary Bypass
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510(K) Number
K082082
Device Name
Reservoir, Blood, Cardiopulmonary Bypass
Applicant
GISH BIOMEDICAL, INC.
22942 ARROYO VISTA
RANCHO SANTA MARGARITA, CA 92688 US
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MARTIN SELLERS
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Regulation Number
870.4400
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Classification Product Code
DTN
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More FDA Info for this Product Code
Date Received
07/23/2008
Decision Date
02/04/2009
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
CV - Cardiovascular
Review Advisory Committee
CV - Cardiovascular
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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