FDA 510(k), K061711, OASIS WOUND MATRIX

FDA 510(k), K061711, OASIS WOUND MATRIX

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510(K) Number: K061711
Device Name: OASIS WOUND MATRIX
Manufacturer: PERRY W GUINN
Device Classification Name: Wound Dressing With Animal-Derived Material(S)
Regulation Number: KGN
Classification Product Code: 06/19/2006
Date Received: 07/19/2006
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery
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