510(k) K222463 ยท QUO Adjunctive Heart Failure Status Indicator
EchoGo Heart Failure
| Applicant | Ultromics Limited, Oxford, GB |
| Decision | Substantially Equivalent, Nov 23, 2022 |
| Received | Aug 15, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K222463
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.