FDA 510(k) Application Details - K072681

Device Classification Name	More FDA Info for this Device
510(K) Number	K072681
Device Name	BLOODSTOP HEMOSTATIC GAUZE; IX HEMOSTATIC GAUZE
Applicant	LIFESCIENCE PLUS, INC. 22 STONY HILL DRIVE MYSTIC, CT 06355 US Other 510(k) Applications for this Company
Contact	AUDRY VITALE Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	QSY Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/21/2007
Decision Date	11/02/2007
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