510(k) K240229 ยท DPS Electrocardiograph
Masimo W1
| Applicant | Masimo Corporation, Irvine CA, US |
| Decision | Substantially Equivalent, Aug 8, 2024 |
| Received | Jan 29, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K240229
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.