510(k) K152973 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
Dyna-Vision Telemonitoring System
| Applicant | Techmedic Development International B.V., Broek Op Langedijk, NL |
| Decision | Substantially Equivalent, Apr 29, 2016 |
| Received | Oct 8, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K152973
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.