510(k) K213657 ยท PJA Coronary Vascular Physiologic Simulation Software
DEEPVESSEL FFR
| Applicant | Keyamed Na, Inc., Seattle WA, US |
| Decision | Substantially Equivalent, Apr 1, 2022 |
| Received | Nov 19, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K213657
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.