FDA 510(k) Application Details - K830936

Device Classification Name Pump, Infusion

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510(K) Number K830936
Device Name Pump, Infusion
Applicant VICKERS AMERICA MEDICAL CORP.

, US
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Regulation Number 880.5725

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Classification Product Code FRN
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Date Received 03/24/1983
Decision Date 04/12/1983
Decision SE - Substantially Equivalent
Classification Advisory Committee HO - General Hospital
Review Advisory Committee HO - General Hospital
Statement / Summary / Purged Status
Type Traditional
Reviewed By Third Party N
Expedited Review



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