FDA 510(k) Application Details - K953008

Device Classification Name	Tube, Feeding   More FDA Info for this Device
510(K) Number	K953008
Device Name	Tube, Feeding
Applicant	MARQUETTE MEDICAL, INC. 1114 BENFIELD BLVD., SUITE K MILLERSVILLE, MD 21108 US Other 510(k) Applications for this Company
Contact	EARL D MARQUETTE, JR. 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	06/28/1995
Decision Date	01/11/1996
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