Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
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
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact