The following data is part of a premarket notification filed by Datex-ohmeda with the FDA for Ge Datex-ohmeda Avance Anesthesia System.
| Device ID | K071142 |
| 510k Number | K071142 |
| Device Name: | GE DATEX-OHMEDA AVANCE ANESTHESIA SYSTEM |
| Classification | Gas-machine, Anesthesia |
| Applicant | DATEX-OHMEDA PO BOX 7550 Madison, WI 53707 |
| Contact | Dan Kosednar |
| Correspondent | Dan Kosednar DATEX-OHMEDA PO BOX 7550 Madison, WI 53707 |
| Product Code | BSZ |
| CFR Regulation Number | 868.5160 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2007-04-24 |
| Decision Date | 2007-06-06 |
| Summary: | summary |