FDA 510(k) Application Details - K161179

Device Classification Name	Cylinder, Compressed Gas, And Valve   More FDA Info for this Device
510(K) Number	K161179
Device Name	Cylinder, Compressed Gas, And Valve
Applicant	AIR LIQUIDE HEALTHCARE AMERICA CORPORATION 12800 West Little York Road HOUSTON, TX 77041-2280 US Other 510(k) Applications for this Company
Contact	Steve Miller 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	04/26/2016
Decision Date	04/13/2017
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