FDA 510(k) Application Details - K992094

Device Classification Name	Dressing,Wound,Hydrogel W/Out Drug And/Or Biologic   More FDA Info for this Device
510(K) Number	K992094
Device Name	Dressing,Wound,Hydrogel W/Out Drug And/Or Biologic
Applicant	GILTECH PLUS, INC. P.O. BOX 728 MILFORD, PA 18337 US Other 510(k) Applications for this Company
Contact	WILLIAM J GILIAM Other 510(k) Applications for this Contact
Regulation Number	878.4022   More FDA Info for this Regulation Number
Classification Product Code	NAE Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/21/1999
Decision Date	09/17/1999
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