FDA 510(k), K122325, SKINTEMP II

FDA 510(k), K122325, SKINTEMP II

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510(K) Number: K122325
Device Name: SKINTEMP II
Manufacturer: JACK SLOVICK
Device Classification Name: Wound Dressing With Animal-Derived Material(S)
Regulation Number: KGN
Classification Product Code: 08/01/2012
Date Received: 10/26/2012
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery

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