FDA 510(k) Application Details - K013936

Device Classification Name	Dressing, Wound, Drug   More FDA Info for this Device
510(K) Number	K013936
Device Name	Dressing, Wound, Drug
Applicant	SILVERLEAF TECHNOLOGIES INC 3 WOODBURN DR. OTTAWA, ONTARIO K1A3B9 CA Other 510(k) Applications for this Company
Contact	ALAN THOMPSON Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	FRO Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/28/2001
Decision Date	03/18/2003
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	-
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review