510(k) K031863 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
CARESTATION 126S VIDEOPHONE
| Applicant | Motion Media Technology, Inc., Wilmington NC, US |
| Decision | Substantially Equivalent, Oct 10, 2003 |
| Received | Jun 16, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K031863
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.