510(k) K082008 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
BIONET BM3PLUS PATIENT MONITOR
| Applicant | Bionet Co., Ltd., San Marino CA, US |
| Decision | Substantially Equivalent, Dec 11, 2008 |
| Received | Jul 15, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K082008
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.