The following data is part of a premarket notification filed by Air Liquide Healthcare with the FDA for Intelli-ox.
| Device ID | K143060 | 
| 510k Number | K143060 | 
| Device Name: | Intelli-Ox | 
| Classification | Cylinder, Compressed Gas, And Valve | 
| Applicant | AIR LIQUIDE HEALTHCARE 2700 POST OAK BLVD., SUITE 325 Houston, TX 77056 | 
| Contact | Angie Beyer | 
| Correspondent | Angie Beyer AIR LIQUIDE HEALTHCARE 2700 POST OAK BLVD., SUITE 325 Houston, TX 77056 | 
| Product Code | ECX | 
| CFR Regulation Number | 868.2700 [🔎] | 
| Decision | Substantially Equivalent (SESE) | 
| Type | Traditional | 
| 3rd Party Reviewed | No | 
| Combination Product | No | 
| Date Received | 2014-10-24 | 
| Decision Date | 2015-05-21 | 
| Summary: | summary | 
| Mark Image Registration | Serial | Company Trademark Application Date | 
|---|---|
|  INTELLI-OX  86263930  5078340 Live/Registered | Air Liquide Healthcare America Corporation 2014-04-27 | 
|  INTELLI-OX  77794658  not registered Dead/Abandoned | Air Liquide Healthcare America Corporation 2009-07-31 |