| K-number | K014188 |
| Device name | NEW PROPHY POWDER |
| Applicant | Dentsply Intl. |
| Product code | KOJ |
| Device class | Class II |
| Decision date | Mar 15, 2002 |
| Decision | Substantially Equivalent |
| Regulation | 872.6080 |
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