FDA 510(k) Application Details - K010797

Device Classification Name	Tubes, Gastrointestinal (And Accessories)   More FDA Info for this Device
510(K) Number	K010797
Device Name	Tubes, Gastrointestinal (And Accessories)
Applicant	RUSCH INTL. 50 PLANTATION DR. JAFFERY, NH 03452 US Other 510(k) Applications for this Company
Contact	JULIE A BEAUMONT Other 510(k) Applications for this Contact
Regulation Number	876.5980   More FDA Info for this Regulation Number
Classification Product Code	KNT Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/16/2001
Decision Date	02/26/2002
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