510(k) K150992 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
Vios Monitoring System
| Applicant | Vios Medical, Inc., St. Paul MN, US |
| Decision | Substantially Equivalent, Dec 16, 2015 |
| Received | Apr 15, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K150992
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.