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 |