510(k) K190090 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
DynoSense Vital Sign Measuring System
| Applicant | Dynosense Corp., Los Gatos CA, US |
| Decision | Substantially Equivalent, Aug 2, 2019 |
| Received | Jan 17, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K190090
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.