Nucletron B.V. · Class II · Cleared Jan 27, 2017
| K-number | K161688 |
| Device name | Advanced Gynecological Applicator |
| Applicant | Nucletron B.V. |
| Product code | JAQ |
| Device class | Class II |
| Decision date | Jan 27, 2017 |
| Decision | Substantially Equivalent |
| Regulation | 892.5700 |
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