FDA 510(k) Application Details - K932221

Device Classification Name	General Surgery Tray   More FDA Info for this Device
510(K) Number	K932221
Device Name	General Surgery Tray
Applicant	ASSOCIATED MEDICAL PRODUCTS CO. 3250 GORHAM AVE. ST. LOUIS PARK, MN 55426 US Other 510(k) Applications for this Company
Contact	SCOTT WEISS 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	05/07/1993
Decision Date	03/19/1997
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