FDA 510(k) Application Details - K963443

Device Classification Name	General Surgery Tray   More FDA Info for this Device
510(K) Number	K963443
Device Name	General Surgery Tray
Applicant	CONTINENTAL MEDICAL LABORATORIES, INC. 817 WEST MOHR AVE. P.O. BOX 306 WATERFORD, WI 53185 US Other 510(k) Applications for this Company
Contact	JOSEPH DUNN Other 510(k) Applications for this Contact
Regulation Number	878.4370   More FDA Info for this Regulation Number
Classification Product Code	LRO Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/30/1996
Decision Date	10/17/1996
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