510(k) K172510 · MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
µCor Heart Failure and Arrhythmia Management System
| Applicant | Zoll Manufacturing Corporation, Pittsburgh PA, US |
| Decision | Substantially Equivalent, May 11, 2018 |
| Received | Aug 21, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172510
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.