K123125 is an FDA 510(k) clearance for the GE DATEX-OHMEDA AVANCE CS2. This device is classified as a Gas-machine, Anesthesia (Class II - Special Controls, product code BSZ).
Submitted by Datex-Ohmeda, Inc. (Madison, US). The FDA issued a Cleared decision on February 6, 2013, 125 days after receiving the submission on October 4, 2012.
This device falls under the Anesthesiology FDA review panel. Regulated under 21 CFR 868.5160.
| 510(k) Number | K123125 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | October 04, 2012 |
| Decision Date | February 06, 2013 |
| Days to Decision | 125 days |
| Submission Type | Special |
| Review Panel | Anesthesiology (AN) |
| Summary | Summary PDF |
| Product Code | BSZ — Gas-machine, Anesthesia |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 868.5160 |