| K-number | K113662 |
| Device name | FENESTRATED NERVE BLOCK NEEDLE |
| Applicant | Imd, Inc. |
| Product code | CAZ |
| Device class | Class II |
| Decision date | Apr 20, 2012 |
| Decision | Substantially Equivalent |
| Regulation | 868.5140 |
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