FDA 510(k) Application Details - K033562

Device Classification Name	Tubes, Gastrointestinal (And Accessories)   More FDA Info for this Device
510(K) Number	K033562
Device Name	Tubes, Gastrointestinal (And Accessories)
Applicant	C.R. BARD, INC. 129 CONCORD ROAD BUILDING 3 BILLERICA, MA 01821 US Other 510(k) Applications for this Company
Contact	THOMAS HIRTE, P.E. 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	11/12/2003
Decision Date	12/12/2003
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	GU - Gastroenterology & Urology
Review Advisory Committee	GU - Gastroenterology & Urology
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review