510(k) K250569 ยท DPS Electrocardiograph
Cardiologs Holter Platform
| Applicant | Philips France Commercial, Paris, FR |
| Decision | Substantially Equivalent, Aug 6, 2025 |
| Received | Feb 26, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K250569
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.