K070109 is an FDA 510(k) clearance for the NEUROMETRIX ADVANCE. This device is classified as a Device, Nerve Conduction Velocity Measurement (Class II - Special Controls, product code JXE).
Submitted by Neurometrix, Inc. (Waltham, US). The FDA issued a Cleared decision on April 25, 2008, 470 days after receiving the submission on January 11, 2007.
This device falls under the Neurology FDA review panel. Regulated under 21 CFR 882.1550.
| 510(k) Number | K070109 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | January 11, 2007 |
| Decision Date | April 25, 2008 |
| Days to Decision | 470 days |
| Submission Type | Traditional |
| Review Panel | Neurology (NE) |
| Summary | Summary PDF |
| Product Code | JXE - Device, Nerve Conduction Velocity Measurement |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 882.1550 |