FDA 510(k) Application Details - K984310

Device Classification Name	Tubes, Gastrointestinal (And Accessories)   More FDA Info for this Device
510(K) Number	K984310
Device Name	Tubes, Gastrointestinal (And Accessories)
Applicant	MOSS TUBES, INC. 304 VERONA AVE. ELIZABETH, NJ 07208 US Other 510(k) Applications for this Company
Contact	HARRY A SCHLAKMAN 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	12/02/1998
Decision Date	02/24/1999
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