FDA 510(k) Application Details - K020732

Device Classification Name	Dressing, Wound, Collagen   More FDA Info for this Device
510(K) Number	K020732
Device Name	Dressing, Wound, Collagen
Applicant	COOK BIOTECH, INC. 3055 KENT AVE. WEST LAFAYETTE, IN 47906-1076 US Other 510(k) Applications for this Company
Contact	MARK BLEYER Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	KGN Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/06/2002
Decision Date	05/30/2002
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	-
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review