510(k) K081444 ยท DSI Detector And Alarm, Arrhythmia
BRAEMAR FUSION WIRELESS - AMBULATORY ECG ARRHYTHMIA MONITORING SYSTEM
| Applicant | Braemar, Inc., Eagan MN, US |
| Decision | Substantially Equivalent, Jul 31, 2008 |
| Received | May 22, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K081444
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.