510(k) K012241 ยท DSI Detector And Alarm, Arrhythmia
CARDIONET AMBULATORY ECG MONITOR WITH ARRHYTHMIA DETECTION, MODEL CN1001
| Applicant | Cardionet, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Feb 1, 2002 |
| Received | Jul 17, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K012241
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.