510(k) K142352 ยท DSI Detector And Alarm, Arrhythmia
CardiacLinx
| Applicant | Ross Medical Technology, Inc., Saddle River NJ, US |
| Decision | Substantially Equivalent, Mar 12, 2015 |
| Received | Aug 22, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K142352
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.