FDA 510(k) Application Details - K841827

Device Classification Name Pump, Infusion

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510(K) Number K841827
Device Name Pump, Infusion
Applicant DIATEK, INC.

, US
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Regulation Number 880.5725

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Classification Product Code FRN
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Date Received 05/03/1984
Decision Date 07/27/1984
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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