K061112 is an FDA 510(k) clearance for the CONMED PRO2 PULSE REFLECTANCE OXIMETER, MODEL PRO-M. This device is classified as a Oximeter (Class II - Special Controls, product code DQA).
Submitted by Conmed Corporation (Utica, US). The FDA issued a Cleared decision on May 22, 2006, 31 days after receiving the submission on April 21, 2006.
This device falls under the Anesthesiology FDA review panel. Regulated under 21 CFR 870.2700.
| 510(k) Number | K061112 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | April 21, 2006 |
| Decision Date | May 22, 2006 |
| Days to Decision | 31 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 |