Technomed Europe · Class II · Cleared Jul 19, 2013
| K-number | K130136 |
| Device name | DISPOSABLE AND REUSABLE CONCENTRIC NEEDLE ELECTRODES,DISPOSABLE AND REUSABLE SUBDERMAL NEEDLE ELECTRODES, |
| Applicant | Technomed Europe |
| Product code | GXZ |
| Device class | Class II |
| Decision date | Jul 19, 2013 |
| Decision | Substantially Equivalent |
| Regulation | 882.1350 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov