510(k) K190468 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
Nihon Kohden SVM-7200 Series Vital Signs Monitor
| Applicant | Nihon Kohden Corporation, Tokyo, JP |
| Decision | Substantially Equivalent, May 28, 2019 |
| Received | Feb 26, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K190468
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.