510(k) K130234 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
NUVON VITALS CHARTING SYSTEM
| Applicant | Nuvon, Inc., Washington DC, US |
| Decision | Substantially Equivalent, Mar 13, 2013 |
| Received | Jan 30, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K130234
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.