FDA 510(k) Application Details - K970889

Device Classification Name	Drape, Surgical   More FDA Info for this Device
510(K) Number	K970889
Device Name	Drape, Surgical
Applicant	PROTEK MEDICAL PRODUCTS, INC. 221 E. MARKET ST. SUITE 291 IOWA CITY, IA 52245 US Other 510(k) Applications for this Company
Contact	RICK L PRUTER Other 510(k) Applications for this Contact
Regulation Number	878.4370   More FDA Info for this Regulation Number
Classification Product Code	KKX Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/11/1997
Decision Date	10/20/1997
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review