510(k) K131000 ยท DSI Detector And Alarm, Arrhythmia
V-PATCH SYSTEM
| Applicant | Intelesens Limited, Bonita Springs FL, US |
| Decision | Substantially Equivalent, Jan 8, 2014 |
| Received | Apr 10, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K131000
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.