510(k) K153079 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
Axeo 3 Patient Monitor
| Applicant | Axeo Medical Technologies, LLC, Palm Harbor FL, US |
| Decision | Substantially Equivalent, Mar 17, 2016 |
| Received | Oct 23, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K153079
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.