510(k) K233354 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
WVSM Pro (Series) (500-0030-XX)
| Applicant | Athena Gtx, Inc., Johnson IA, US |
| Decision | Substantially Equivalent, Jun 26, 2024 |
| Received | Sep 29, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K233354
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.