510(k) K231600 ยท DQY Catheter, Percutaneous
SENDERO Microcatheter
| Applicant | Okami Medical, Inc., Aliso Viejo CA, US |
| Decision | Substantially Equivalent, Nov 17, 2023 |
| Received | Jun 1, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K231600
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.