K121012 is an FDA 510(k) clearance for the FLEXLAB 3.6, ACCELERATOR A3600. This device is classified as a Electrode, Ion Specific, Potassium (Class II - Special Controls, product code CEM).
Submitted by Inpeco S.P.A. (Segrate, Milan, IT). The FDA issued a Cleared decision on August 31, 2012, 150 days after receiving the submission on April 3, 2012.
This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 862.1600.
| 510(k) Number | K121012 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | April 03, 2012 |
| Decision Date | August 31, 2012 |
| Days to Decision | 150 days |
| Submission Type | Traditional |
| Review Panel | Chemistry (CH) |
| Summary | Summary PDF |
| Product Code | CEM — Electrode, Ion Specific, Potassium |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 862.1600 |