FDA 510(k) Application Details - K073288

Device Classification Name	Snare, Flexible   More FDA Info for this Device
510(K) Number	K073288
Device Name	Snare, Flexible
Applicant	ETHICON ENDO-SURGERY, INC. 4545 CREEK RD. CINCINNATI, OH 45242-2839 US Other 510(k) Applications for this Company
Contact	GLENDA C MARSH Other 510(k) Applications for this Contact
Regulation Number	876.4300   More FDA Info for this Regulation Number
Classification Product Code	FDI Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/21/2007
Decision Date	06/12/2008
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