FDA 510(k) Application Details - K992477

Device Classification Name	Snare, Flexible   More FDA Info for this Device
510(K) Number	K992477
Device Name	Snare, Flexible
Applicant	INSCOPE, LLC. 19526 EAST LAKE DR. MIAMI, FL 33015 US Other 510(k) Applications for this Company
Contact	AL WEISENBORN 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	07/26/1999
Decision Date	08/24/1999
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