510(k) K100217 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
LUCON M-SERIES PATIENT MONITOR, MODELS M20 AND M30
| Applicant | Mediana Co., Ltd., Echo OR, US |
| Decision | Substantially Equivalent, Jun 8, 2010 |
| Received | Jan 25, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K100217
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.