The following data is part of a premarket notification filed by Siemens Elema Ab with the FDA for Siemens-elema Ab O2-air Mixer 960.
| Device ID | K800905 |
| 510k Number | K800905 |
| Device Name: | SIEMENS-ELEMA AB O2-AIR MIXER 960 |
| Classification | Mixer, Breathing Gases, Anesthesia Inhalation |
| Applicant | SIEMENS ELEMA AB 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | BZR |
| CFR Regulation Number | 868.5330 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1980-04-21 |
| Decision Date | 1980-05-08 |