510(k) K214024 ยท DQY Catheter, Percutaneous
SOFIA 88 Catheter
| Applicant | MicroVention, Inc., Aliso Viejo CA, US |
| Decision | Substantially Equivalent, Sep 12, 2022 |
| Received | Dec 22, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K214024
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.