510(k) K242420 ยท DQO Catheter, Intravascular, Diagnostic
pNOVUS 21 Microcatheter
| Applicant | Phenox, Ltd., Galway, IE |
| Decision | Substantially Equivalent, Nov 12, 2024 |
| Received | Aug 15, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K242420
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.