510(k) K010424 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
NEXAN SYSTEM, MODEL NX-301
| Applicant | Nexan, Ltd., Rockville MD, US |
| Decision | Substantially Equivalent, Sep 4, 2001 |
| Received | Feb 13, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K010424
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.