FDA 510(k) Application Details - K840914

Device Classification Name Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass

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510(K) Number K840914
Device Name Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
Applicant SHERWOOD MEDICAL CO.

, US
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Regulation Number 870.4210

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Classification Product Code DWF
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Date Received 02/29/1984
Decision Date 04/17/1984
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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