Intervene · Class II · Cleared Oct 22, 2025
| K-number | K251185 |
| Device name | Recana Thrombectomy Catheter System (FG014. FG015, FG016, FG017, FG018, FG019, FG020) |
| Applicant | Intervene |
| Product code | QEW |
| Device class | Class II |
| Decision date | Oct 22, 2025 |
| Decision | Substantially Equivalent |
| Regulation | 870.5150 |
The FDA summary PDF for this submission is not available in machine-readable form — common for older clearances. View on FDA's site →
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