Ximed/Prosure/Injectx · Class II · Cleared Dec 11, 1998
| K-number | K983765 |
| Device name | INJECTION NEEDLE PROBE/DEVICE-TUNIS |
| Applicant | Ximed/Prosure/Injectx |
| Product code | FBK |
| Device class | Class II |
| Decision date | Dec 11, 1998 |
| Decision | Substantially Equivalent |
| Regulation | 876.1500 |
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