The following data is part of a premarket notification filed by Chambers & Sadler Mfg. with the FDA for Oxy-on Digital Oxygen Timer.
| Device ID | K781039 |
| 510k Number | K781039 |
| Device Name: | OXY-ON DIGITAL OXYGEN TIMER |
| Classification | Transducer, Gas Flow |
| Applicant | CHAMBERS & SADLER MFG. 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 | 1978-06-19 |
| Decision Date | 1978-08-31 |