FDA 510(k) Application Details - K131386

Device Classification Name	Cylinder, Compressed Gas, And Valve   More FDA Info for this Device
510(K) Number	K131386
Device Name	Cylinder, Compressed Gas, And Valve
Applicant	AIR LIQUIDE HEALTHCARE AMERICA 2700 POST OAK BLVD. SUITE 1800 HOUSTON, TX 77056 US Other 510(k) Applications for this Company
Contact	ANGIE BEYER Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	ECX Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/14/2013
Decision Date	03/14/2014
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review