510(k) K253436 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
c-med0 alpha
| Applicant | Cosinuss GmbH, Munich, DE |
| Decision | Substantially Equivalent, Apr 30, 2026 |
| Received | Oct 1, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K253436
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.