The following data is part of a premarket notification filed by Air Liquide Healthcare America with the FDA for Ez-ox Plus.
| Device ID | K053117 | 
| 510k Number | K053117 | 
| Device Name: | EZ-OX PLUS | 
| Classification | Cylinder, Compressed Gas, And Valve | 
| Applicant | AIR LIQUIDE HEALTHCARE AMERICA 2700 POST OAK BLVD. SUITE 1800 Houston, TX 77056 | 
| Contact | Angie Beyer | 
| Correspondent | Angie Beyer AIR LIQUIDE HEALTHCARE AMERICA 2700 POST OAK BLVD. SUITE 1800 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 | 2005-11-07 | 
| Decision Date | 2006-04-10 | 
| Summary: | summary | 
| Mark Image Registration | Serial | Company Trademark Application Date | 
|---|---|
|  EZ-OX PLUS  78364575  3330509 Live/Registered | Air Liquide America, LP 2004-02-09 |