| K-number | K031793 |
| Device name | DENTATUS OSCIOMAT |
| Applicant | Dentatus USA , Ltd. |
| Product code | DZH |
| Device class | Class II |
| Decision date | Nov 13, 2003 |
| Decision | Substantially Equivalent |
| Regulation | 872.4120 |
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