510(k) K232495 ยท DQA Oximeter
Sempulse Halo Vital Signs Monitor
| Applicant | Sempulse Corporation, San Marcos TX, US |
| Decision | Substantially Equivalent, May 16, 2024 |
| Received | Aug 17, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K232495
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.