| K-number | K882404 |
| Device name | KEVOR-CURETTE |
| Applicant | Euro-Med Intl. |
| Product code | PCF |
| Device class | Class II |
| Decision date | Jul 8, 1988 |
| Decision | Substantially Equivalent |
| Regulation | 884.1050 |
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