| K-number | K973340 |
| Device name | TWEEZER-TYPE EPILATOR |
| Applicant | Mobit, Inc. |
| Product code | KCX |
| Device class | Class I |
| Decision date | Dec 3, 1997 |
| Decision | Substantially Equivalent |
| Regulation | 878.5360 |
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