510(k) K213666 ยท DQO Catheter, Intravascular, Diagnostic
NuCath Wedge Pressure Catheter
| Applicant | Pfm Medical, Inc., Carlsbad CA, US |
| Decision | Substantially Equivalent, Oct 6, 2022 |
| Received | Nov 22, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K213666
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.