510(k) K001693 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
LIFE SCOPE P, MODEL BSM-4100 SERIES
| Applicant | Nihon Kohden America, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Oct 24, 2000 |
| Received | Jun 2, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K001693
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.