510(k) K230375 ยท MXD Recorder, Event, Implantable Cardiac, (With Arrhythmia Detection)
BIOMONITOR IV
| Applicant | Biotronik, Inc., Lake Oswego OR, US |
| Decision | Substantially Equivalent, May 19, 2023 |
| Received | Feb 13, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K230375
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.