FDA 510(k) Application Details - K952262

Device Classification Name	Ligator, Hemorrhoidal   More FDA Info for this Device
510(K) Number	K952262
Device Name	Ligator, Hemorrhoidal
Applicant	BOSTON SCIENTIFIC CORP. ONE BOSTON SCIENTIFIC PL. NATICK, MA 01760-1537 US Other 510(k) Applications for this Company
Contact	DANIEL J DILLON 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	05/15/1995
Decision Date	02/29/1996
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