510(k) K130709 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, Oct 7, 2013 |
| Received | Mar 15, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K130709
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.