510(k) K090834 ยท DSI Detector And Alarm, Arrhythmia
EPICARDIA 5000
| Applicant | Medicomp, Inc., Great Neck NY, US |
| Decision | Substantially Equivalent, May 15, 2009 |
| Received | Mar 27, 2009 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K090834
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.