FDA 510(k), K963141, KUGEL HERNIA PATCH

FDA 510(k), K963141, KUGEL HERNIA PATCH

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510(K) Number: K963141
Device Name: KUGEL HERNIA PATCH
Manufacturer: Douglas Bueschel
Device Classification Name: Mesh, Surgical, Polymeric
Regulation Number: FTL
Classification Product Code: KXA
Date Received: 08/13/1996
Decision Date: 10/11/1996
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery
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