FDA 510(k) Application Details - K992719

Device Classification Name	Tubes, Gastrointestinal (And Accessories)   More FDA Info for this Device
510(K) Number	K992719
Device Name	Tubes, Gastrointestinal (And Accessories)
Applicant	AMSINO INTL., INC. 833 TOWNE CENTER DR. POMONA, CA 91767 US Other 510(k) Applications for this Company
Contact	RICHARD Y LI 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	08/12/1999
Decision Date	01/12/2000
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