K111378 is an FDA 510(k) clearance for the OXIMETRY INTERFACE KIT. This device is classified as a Ventilator, Continuous, Non-life-supporting (Class II - Special Controls, product code MNS).
Submitted by Philips Respironics, Inc. (Murrysville, US). The FDA issued a Cleared decision on October 4, 2011, 140 days after receiving the submission on May 17, 2011.
This device falls under the Anesthesiology FDA review panel. Regulated under 21 CFR 868.5895.
| 510(k) Number | K111378 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | May 17, 2011 |
| Decision Date | October 04, 2011 |
| Days to Decision | 140 days |
| Submission Type | Traditional |
| Review Panel | Anesthesiology (AN) |
| Summary | Summary PDF |
| Product Code | MNS — Ventilator, Continuous, Non-life-supporting |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 868.5895 |