FDA 510(k), K022782, DUALMESH EMERGE & EMERGE PLUS BIOMATERIAL

FDA 510(k), K022782, DUALMESH EMERGE & EMERGE PLUS BIOMATERIAL

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510(K) Number: K022782
Device Name: DUALMESH EMERGE & EMERGE PLUS BIOMATERIAL
Manufacturer:
Device Classification Name: Mesh, Surgical, Polymeric
Regulation Number: 878.3300
Classification Product Code: FTL
Date Received: 08/22/2002
Decision Date: 09/10/2002
Regulation Medical Specialty: General & Plastic Surgery
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