FDA 510(k) Application Details - K963724

Device Classification Name	Gauze/Sponge, Internal   More FDA Info for this Device
510(K) Number	K963724
Device Name	Gauze/Sponge, Internal
Applicant	GRAND MEDICAL PRODUCTS 1300 REMINGTON ROAD, SUITE K SCHAUMBURG, IL 60173 US Other 510(k) Applications for this Company
Contact	HARVEY WEISS Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	EFQ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/16/1996
Decision Date	11/29/1996
Decision	SN - Substantially Equivalent for Some Indications
Classification Advisory Committee	-
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status
Type	Traditional
Reviewed By Third Party	N
Expedited Review