K072201 is an FDA 510(k) clearance for the COMPUMEDICS SOMTE PSG RECORDING SYSTEM. This device is classified as a Ventilatory Effort Recorder (Class II - Special Controls, product code MNR).
Submitted by Compumedics Limited (Melbourne, Victoria, AU). The FDA issued a Cleared decision on April 14, 2008, 250 days after receiving the submission on August 8, 2007.
This device falls under the Anesthesiology FDA review panel. Regulated under 21 CFR 868.2375.
| 510(k) Number | K072201 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | August 08, 2007 |
| Decision Date | April 14, 2008 |
| Days to Decision | 250 days |
| Submission Type | Traditional |
| Review Panel | Anesthesiology (AN) |
| Summary | Summary PDF |
| Product Code | MNR - Ventilatory Effort Recorder |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 868.2375 |