K072131 is an FDA 510(k) clearance for the M3 MONITOR. This device is classified as a Monitor, Blood-gas, On-line, Cardiopulmonary Bypass (Class II - Special Controls, product code DRY).
Submitted by Spectrum Medical , Ltd. (Gloucester, Gloucesterhsire, GB). The FDA issued a Cleared decision on August 17, 2007, 15 days after receiving the submission on August 2, 2007.
This device falls under the Cardiovascular FDA review panel. Regulated under 21 CFR 870.4330.
| 510(k) Number | K072131 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | August 02, 2007 |
| Decision Date | August 17, 2007 |
| Days to Decision | 15 days |
| Submission Type | Traditional |
| Review Panel | Cardiovascular (CV) |
| Summary | Summary PDF |
| Product Code | DRY — Monitor, Blood-gas, On-line, Cardiopulmonary Bypass |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 870.4330 |