510(k) K173170 ยท DSI Detector And Alarm, Arrhythmia
Epicardia Anywhere
| Applicant | Medicomp, Inc., Melbourne FL, US |
| Decision | Substantially Equivalent, Jan 10, 2018 |
| Received | Sep 29, 2017 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K173170
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.