510(k) K170538 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
RVS-100 Vital Signs Monitor
| Applicant | Rudolf Riester GmbH, Jungingen, DE |
| Decision | Substantially Equivalent, Oct 17, 2017 |
| Received | Feb 23, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K170538
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.