510(k) K241894 · QEW Peripheral Mechanical Thrombectomy With Aspiration
Artix MT; Artix Thin-Walled Thrombectomy Sheath
| Applicant | Inari Medical, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Oct 15, 2024 |
| Received | Jun 28, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K241894
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| May 6, 2025 | Inari Medical - Oak Canyon Artix MT Thrombectomy Device, REF: 32-102 Open, Classified |
QEW | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.