FDA 510(k) Application Details - K803037

Device Classification Name Apparatus, Suction, Patient Care

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510(K) Number K803037
Device Name Apparatus, Suction, Patient Care
Applicant C.R. BARD, INC.

, US
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Regulation Number 870.5050

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Classification Product Code DWM
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Date Received 12/01/1980
Decision Date 02/04/1981
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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