K173815 is an FDA 510(k) clearance for the Allergan Botox Needle Electrode. This device is classified as a Electrode, Needle, Diagnostic Electromyograph (Class II - Special Controls, product code IKT).
Submitted by Natus Manufacturing Limited (Gort, IE). The FDA issued a Cleared decision on June 29, 2018, 196 days after receiving the submission on December 15, 2017.
This device falls under the Neurology FDA review panel. Regulated under 21 CFR 890.1385.
| 510(k) Number | K173815 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | December 15, 2017 |
| Decision Date | June 29, 2018 |
| Days to Decision | 196 days |
| Submission Type | Traditional |
| Review Panel | Neurology (NE) |
| Summary | Summary PDF |
| Product Code | IKT - Electrode, Needle, Diagnostic Electromyograph |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 890.1385 |