FDA 510(k), K033337, ULTRAPRO MESH

FDA 510(k), K033337, ULTRAPRO MESH

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510(K) Number: K033337
Device Name: ULTRAPRO MESH
Manufacturer: ETHICON, INC.
Device Classification Name: mesh, surgical, polymeric
Regulation Number: 878.3300
Classification Product Code: FTL
Date Received: 10/17/2003
Decision Date: 04/01/2004
Regulation Medical Specialty: General & Plastic Surgery
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