510(k) K102135 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
VECTOR EVENT GRID ARCHITECTURE (VEGA) SYSTEM
| Applicant | Nuvon, Inc., Washington DC, US |
| Decision | Substantially Equivalent, Oct 22, 2010 |
| Received | Jul 29, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K102135
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.