K924127 is an FDA 510(k) clearance for the DANTEC EVOLUTION. This device is classified as a Stimulator, Electrical, Evoked Response (Class II - Special Controls, product code GWF).
Submitted by Dantec Medical, Inc. (Washington, US). The FDA issued a Cleared decision on March 10, 1993, 205 days after receiving the submission on August 17, 1992.
This device falls under the Neurology FDA review panel. Regulated under 21 CFR 882.1870.
| 510(k) Number | K924127 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | August 17, 1992 |
| Decision Date | March 10, 1993 |
| Days to Decision | 205 days |
| Submission Type | Traditional |
| Review Panel | Neurology (NE) |
| Summary | Summary PDF |
| Product Code | GWF — Stimulator, Electrical, Evoked Response |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 882.1870 |