| K-number | K024190 |
| Device name | FENESTRATED INFUSION CATHETER |
| Applicant | Promedic, Inc. |
| Product code | FRN |
| Device class | Class II |
| Decision date | Mar 17, 2003 |
| Decision | Substantially Equivalent |
| Regulation | 880.5725 |
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