510(k) K132033 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
BM3/BM3 PLUS
| Applicant | Noblitt & Rueland, Irvine CA, US |
| Decision | Substantially Equivalent, Dec 4, 2013 |
| Received | Jul 1, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K132033
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.