FDA 510(k) Application Details - K973892

Device Classification Name	Tubes, Gastrointestinal (And Accessories)   More FDA Info for this Device
510(K) Number	K973892
Device Name	Tubes, Gastrointestinal (And Accessories)
Applicant	RUSCH INTL. TALL PINES PARK JAFFREY, NH 03452 US Other 510(k) Applications for this Company
Contact	JAMES R WHITNEY 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	10/14/1997
Decision Date	05/18/1998
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