510(k) K221856 ยท MXD Recorder, Event, Implantable Cardiac, (With Arrhythmia Detection)
BIOMONITOR IIIm, BIOMONITOR III
| Applicant | Biotronik, Inc., Lake Oswego OR, US |
| Decision | Substantially Equivalent, Jul 27, 2022 |
| Received | Jun 27, 2022 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K221856
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.