FDA 510(k), K982532, PARIETEX

FDA 510(k), K982532, PARIETEX

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510(K) Number: K982532
Device Name: PARIETEX
Manufacturer: HOWARD M HOLSTEIN
Device Classification Name: Mesh, Surgical, Polymeric
Regulation Number: FTL
Classification Product Code: KXA
Date Received: 07/20/1998
Decision Date: 01/20/1999
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery
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