K092793 is an FDA 510(k) clearance for the MODIFICATION TO:KNEEHAB XP CONDUCTIVE GARMENT, MODEL 411. 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 December 7, 2009, 87 days after receiving the submission on September 11, 2009.
This device falls under the Neurology FDA review panel. Regulated under 21 CFR 882.1320.
| 510(k) Number | K092793 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | September 11, 2009 |
| Decision Date | December 07, 2009 |
| Days to Decision | 87 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 |