FDA 510(k) Application Details - K091519

Device Classification Name	Ligator, Hemorrhoidal   More FDA Info for this Device
510(K) Number	K091519
Device Name	Ligator, Hemorrhoidal
Applicant	HAEMOBAND SURGICAL LTD. 24301 WOODSAGE DRIVE BONITA SPRINGS, FL 34134 US Other 510(k) Applications for this Company
Contact	PAUL DRYDEN Other 510(k) Applications for this Contact
Regulation Number	876.4400   More FDA Info for this Regulation Number
Classification Product Code	FHN Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/22/2009
Decision Date	07/28/2009
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	GU - Gastroenterology & Urology
Review Advisory Committee	GU - Gastroenterology & Urology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review