510(k) K010923 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
KION ANAESTHESIA SYSTEM, MODEL 65 03 879 E392E
| Applicant | Siemens Elema AB, Iselin NJ, US |
| Decision | Substantially Equivalent, Jan 23, 2002 |
| Received | Mar 27, 2001 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K010923
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.