510(k) K252361 ยท DPS Electrocardiograph
AccurECG Analysis System (v2.0)
| Applicant | Accurkardia, Inc., New York NY, US |
| Decision | Substantially Equivalent, Dec 22, 2025 |
| Received | Jul 29, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K252361
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.