K011670 is an FDA 510(k) clearance for the DATEX-OHMEDA OXYGEN SATURATION MODULE, M-OSAT AND ACCESSORIES (WITH TRUTRAK+MOTION CORRECTION PERFORMANCE. This device is classified as a Oximeter (Class II - Special Controls, product code DQA).
Submitted by Datex-Ohmeda (Tewksbury, US). The FDA issued a Cleared decision on June 26, 2001, 27 days after receiving the submission on May 30, 2001.
This device falls under the Anesthesiology FDA review panel. Regulated under 21 CFR 870.2700.
| 510(k) Number | K011670 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | May 30, 2001 |
| Decision Date | June 26, 2001 |
| Days to Decision | 27 days |
| Submission Type | Special |
| Review Panel | Anesthesiology (AN) |
| Summary | Summary PDF |
| Product Code | DQA — Oximeter |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 870.2700 |