Uresil Corp. · Class II · Cleared Jan 2, 1987
| K-number | K864007 |
| Device name | EMBOLECTOMY/THROMBECTOMY BALLOON CATHETER |
| Applicant | Uresil Corp. |
| Product code | DXE |
| Device class | Class II |
| Decision date | Jan 2, 1987 |
| Decision | Substantially Equivalent |
| Regulation | 870.5150 |
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