510(k) K221846 ยท DQY Catheter, Percutaneous
Artix Ballon Guiding Sheath
| Applicant | Inari Medical, Irvine CA, US |
| Decision | Substantially Equivalent, Jul 11, 2022 |
| Received | Jun 24, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K221846
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.