| K-number | K991259 |
| Device name | TE ME NA EPIDURAL CATHETER |
| Applicant | Te ME NA S.A.R.L. |
| Product code | BSO |
| Device class | Class II |
| Decision date | Feb 21, 2001 |
| Decision | Substantially Equivalent |
| Regulation | 868.5120 |
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