510(k) K243566 · DXR Ballistocardiograph
CardioTag
| Applicant | Cardiosense, Inc., Chicago IL, US |
| Decision | Substantially Equivalent, Jul 22, 2025 |
| Received | Nov 18, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K243566
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.