The following data is part of a premarket notification filed by The John Bunn Co. with the FDA for Arizona Oxygen Timer Device.
| Device ID | K761260 |
| 510k Number | K761260 |
| Device Name: | ARIZONA OXYGEN TIMER DEVICE |
| Classification | Transducer, Gas Flow |
| Applicant | THE JOHN BUNN CO. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | BXP |
| CFR Regulation Number | 868.2885 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1976-12-08 |
| Decision Date | 1976-12-16 |