510(k) K171056 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
WAVE Clinical Platform
| Applicant | Excel Medical Electronics, LLC, Jupiter FL, US |
| Decision | Substantially Equivalent, Jan 4, 2018 |
| Received | Apr 10, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K171056
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.