510(k) K240384 ยท DQY Catheter, Percutaneous
SENDERO Microcatheter
| Applicant | Okami Medical, Inc., Aliso Viejo CA, US |
| Decision | Substantially Equivalent, Mar 8, 2024 |
| Received | Feb 8, 2024 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K240384
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.