510(k) K012226 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
MONITORING SYSTEM,MODEL ARGUS PB-1000
| Applicant | Schiller AG, Baar, CH |
| Decision | Substantially Equivalent, Apr 8, 2002 |
| Received | Jul 16, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K012226
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.