510(k) K181658 ยท DSI Detector And Alarm, Arrhythmia
MobileECG 2 BT
| Applicant | Memtec Corporation, Salem NH, US |
| Decision | Substantially Equivalent, Mar 26, 2019 |
| Received | Jun 25, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K181658
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.