FDA 510(k), K103682, PARIETEX PROGRIP

FDA 510(k), K103682, PARIETEX PROGRIP

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510(K) Number: K103682
Device Name: PARIETEX PROGRIP
Manufacturer: JAMES MCMAHON
Device Classification Name: Mesh, Surgical, Polymeric
Regulation Number: FTL
Classification Product Code: 12/17/2010
Date Received: 03/04/2011
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery

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