FDA 510(k) Application Details - K840915

Device Classification Name Container, I.V.

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510(K) Number K840915
Device Name Container, I.V.
Applicant GIL-MED INDUSTRIES C/O KEGAN & KEGAN, LTD.

, US
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Regulation Number 880.5025

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