| K-number | K042870 |
| Device name | ENDO TWINN |
| Applicant | Endo Twinn B.V. |
| Product code | EKM |
| Device class | Class I |
| Decision date | Jan 11, 2005 |
| Decision | Substantially Equivalent |
| Regulation | 872.3850 |
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