FDA 510(k) Application Details - K030784

Device Classification Name	Tubes, Gastrointestinal (And Accessories)   More FDA Info for this Device
510(K) Number	K030784
Device Name	Tubes, Gastrointestinal (And Accessories)
Applicant	APPLIED MEDICAL TECHNOLOGY, INC. 15653 NEO PKWY. CLEVELAND, OH 44128 US Other 510(k) Applications for this Company
Contact	CHRIS ZANTOPULOS 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	03/12/2003
Decision Date	04/01/2004
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