510(k) K160899 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
CoVa Monitoring System 2
| Applicant | Tosense, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Jun 22, 2017 |
| Received | Apr 1, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K160899
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.