510(k) K152341 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
ViSi Mobile Monitoring System
| Applicant | Sotera Wireless, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Dec 14, 2015 |
| Received | Aug 19, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K152341
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.