K122944 is an FDA 510(k) clearance for the GEMORE TRUE SINE INTERFERENTIAL STIMULATOR. This device is classified as a Interferential Current Therapy (Class II - Special Controls, product code LIH).
Submitted by Gemore Technology Co, Ltd. (Tan Shui, New Taipei City, TW). The FDA issued a Cleared decision on December 21, 2012, 88 days after receiving the submission on September 24, 2012.
This device falls under the Neurology FDA review panel. Regulated under 21 CFR 882.5890.
| 510(k) Number | K122944 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | September 24, 2012 |
| Decision Date | December 21, 2012 |
| Days to Decision | 88 days |
| Submission Type | Special |
| Review Panel | Neurology (NE) |
| Summary | Summary PDF |
| Product Code | LIH - Interferential Current Therapy |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 882.5890 |