510(k) K230286 · MXC Recorder, Event, Implantable Cardiac, (Without Arrhythmia Detection)
Assert-IQ Insertable Cardiac Monitor
| Applicant | ABBOTT MEDICAL, Sylmar CA, US |
| Decision | Substantially Equivalent, May 17, 2023 |
| Received | Feb 2, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K230286
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.