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FDA 510(k) Application Details - K073631
Device Classification Name
Pump, Blood, Cardiopulmonary Bypass, Non-Roller Type
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510(K) Number
K073631
Device Name
Pump, Blood, Cardiopulmonary Bypass, Non-Roller Type
Applicant
ORQIS MEDICAL CORPORATION
14 ORCHARD ROAD, SUITE 100
LAKE FOREST, CA 92630 US
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Contact
RYAN KELLY
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Regulation Number
870.4360
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Classification Product Code
KFM
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More FDA Info for this Product Code
Date Received
12/26/2007
Decision Date
06/27/2008
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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