FDA 510(k) Application Details - K962227

Device Classification Name	Gauze/Sponge, Internal   More FDA Info for this Device
510(K) Number	K962227
Device Name	Gauze/Sponge, Internal
Applicant	NETWORK TRADING CORP. DBA GRAND INTL. 7222 ERTEL LN. HOUSTON, TX 77040 US Other 510(k) Applications for this Company
Contact	DERICK LI 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	06/10/1996
Decision Date	08/19/1996
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