FDA 510(k) Application Details - K113719

Device Classification Name	Tubes, Gastrointestinal (And Accessories)   More FDA Info for this Device
510(K) Number	K113719
Device Name	Tubes, Gastrointestinal (And Accessories)
Applicant	ABBOTT LABORATORIES 3300 STELZER ROAD COLUMBUS, OH 43219-3034 US Other 510(k) Applications for this Company
Contact	ELIZABETH M ZOLA 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	12/19/2011
Decision Date	04/20/2012
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	GU - Gastroenterology & Urology
Review Advisory Committee	GU - Gastroenterology & Urology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review