K912030 is an FDA 510(k) clearance for the CDI(TM) 2000 BLOOD GAS MONITORING SYST, MODIFIED. This device is classified as a Analyzer, Ion, Hydrogen-ion (ph), Blood-phase, Indwelling (Class II - Special Controls, product code CBZ).
Submitted by 3M Company (Tustin, US). The FDA issued a Cleared decision on October 30, 1991, 176 days after receiving the submission on May 7, 1991.
This device falls under the Anesthesiology FDA review panel. Regulated under 21 CFR 868.1170.
| 510(k) Number | K912030 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | May 07, 1991 |
| Decision Date | October 30, 1991 |
| Days to Decision | 176 days |
| Submission Type | Traditional |
| Review Panel | Anesthesiology (AN) |
| Summary | Statement |
| Product Code | CBZ — Analyzer, Ion, Hydrogen-ion (ph), Blood-phase, Indwelling |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 868.1170 |