FDA 510(k) Application Details - K972437

Device Classification Name	Tube, Feeding   More FDA Info for this Device
510(K) Number	K972437
Device Name	Tube, Feeding
Applicant	ROSS PRODUCTS 625 CLEVELAND AVE. COLUMBUS, OH 43215-1724 US Other 510(k) Applications for this Company
Contact	DANIEL HAMILTON Other 510(k) Applications for this Contact
Regulation Number	876.5980   More FDA Info for this Regulation Number
Classification Product Code	FPD Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/30/1997
Decision Date	01/26/1998
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	GU - Gastroenterology & Urology
Review Advisory Committee	GU - Gastroenterology & Urology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review