510(k) K033711 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
FUKUDA DENSHI DYNASCOPE MODEL DS-5000 CENTRAL TELEMETRY SYSTEM
| Applicant | Fukuda Denshi USA, Inc., Redmond WA, US |
| Decision | Substantially Equivalent, Jun 3, 2004 |
| Received | Nov 26, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K033711
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.