K112934 is an FDA 510(k) clearance for the NEUROTECH RECOVERY. This device is classified as a Electrode, Cutaneous (Class II - Special Controls, product code GXY).
Submitted by Bio-Medical Research, Ltd. (Galway, IE). The FDA issued a Cleared decision on January 20, 2012, 109 days after receiving the submission on October 3, 2011.
This device falls under the Neurology FDA review panel. Regulated under 21 CFR 882.1320.
| 510(k) Number | K112934 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | October 03, 2011 |
| Decision Date | January 20, 2012 |
| Days to Decision | 109 days |
| Submission Type | Traditional |
| Review Panel | Neurology (NE) |
| Summary | Summary PDF |
| Product Code | GXY — Electrode, Cutaneous |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 882.1320 |