510(k) K972242 ยท MXC Recorder, Event, Implantable Cardiac, (Without Arrhythmia Detection)
REVEAL INSERTABLE LOOP RECORDER (ILR) SYSTEM
| Applicant | Medtronic Vascular, Minneapolis MN, US |
| Decision | Substantially Equivalent - Subject to Tracking Reg., Jan 16, 1998 |
| Received | Jun 16, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K972242
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.