FDA 510(k) Application Details - K092712

Device Classification Name	Bandage, Liquid   More FDA Info for this Device
510(K) Number	K092712
Device Name	Bandage, Liquid
Applicant	LODESTAR PRODUCTS, INC. 6833 SAINT LAWRENCE ST. PLANO, TX 75024 US Other 510(k) Applications for this Company
Contact	ERIC LUO Other 510(k) Applications for this Contact
Regulation Number	880.5090   More FDA Info for this Regulation Number
Classification Product Code	KMF Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/03/2009
Decision Date	02/23/2010
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review