FDA 510(k) Application Details - K963723

Device Classification Name	Tray, Surgical   More FDA Info for this Device
510(K) Number	K963723
Device Name	Tray, Surgical
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	878.4800   More FDA Info for this Regulation Number
Classification Product Code	LRP Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/16/1996
Decision Date	11/27/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review