FDA 510(k) Application Details - K896974

Device Classification Name Controller, Temperature, Cardiopulmonary Bypass

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510(K) Number K896974
Device Name Controller, Temperature, Cardiopulmonary Bypass
Applicant DAILY MEDICAL PRODUCTS, INC.
3665 KEARNY VILLA RD.
STE 301
SAN DIEGO, CA US
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Contact ALAN SECORD
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Regulation Number 870.4250

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Classification Product Code DWC
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Date Received 12/13/1989
Decision Date 02/05/1990
Decision SE - Substantially Equivalent
Classification Advisory Committee CV - Cardiovascular
Review Advisory Committee CV - Cardiovascular
Statement / Summary / Purged Status
Type Traditional
Reviewed By Third Party N
Expedited Review



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