FDA 510(k) Application Details - K963753

Device Classification Name	Dressing, Wound And Burn, Occlusive   More FDA Info for this Device
510(K) Number	K963753
Device Name	Dressing, Wound And Burn, Occlusive
Applicant	NORTH AMERICAN STERILIZATION & PACKAGING CO. 18 WHITE LAKE RD. P.O. BOX 558 SPARTA, NJ 07871 US Other 510(k) Applications for this Company
Contact	CHARLES E MEISCH Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	MGP Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/18/1996
Decision Date	11/29/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	-
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review