FDA 510(k) Application Details - K963603

Device Classification Name	Bandage, Liquid   More FDA Info for this Device
510(K) Number	K963603
Device Name	Bandage, Liquid
Applicant	DERMA SCIENCES, INC. 121 WEST GRACE ST. OLD FORGE, PA 18518 US Other 510(k) Applications for this Company
Contact	MARK G CLARK Other 510(k) Applications for this Contact
Regulation Number	880.5090   More FDA Info for this Regulation Number
Classification Product Code	KMF Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/09/1996
Decision Date	11/27/1996
Decision	SN - Substantially Equivalent for Some Indications
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status
Type	Traditional
Reviewed By Third Party	N
Expedited Review