510(k) K053207 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
ARGUS, MODEL LCM
| Applicant | Schiller AG, Baar, CH |
| Decision | Substantially Equivalent, May 19, 2006 |
| Received | Nov 16, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K053207
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.