510(k) K040395 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
CENTRAL TELEMETRY SYSTEM, MODEL WEP-4200A SERIES
| Applicant | Nihon Kohden America, Inc., Foothill CA, US |
| Decision | Substantially Equivalent, Jun 1, 2004 |
| Received | Feb 17, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K040395
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.