510(k) K001433 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
CNS-9300 SERIES CENTRAL STATION
| Applicant | Nihon Kohden America, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Nov 7, 2000 |
| Received | May 8, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K001433
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.