| K-number | K973876 |
| Device name | PROPHYFLEX 2, MODEL 2012 |
| Applicant | Kavo America |
| Product code | EFB |
| Device class | Class I |
| Decision date | Dec 19, 1997 |
| Decision | Substantially Equivalent |
| Regulation | 872.4200 |
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