510(k) K842123 ยท DSI Detector And Alarm, Arrhythmia
PERSONAL CL SINGLE-CHANNEL ELECTROCAR
| Applicant | Parexel Intl. Corp., Cambridge MA, US |
| Decision | Substantially Equivalent, Nov 16, 1984 |
| Received | May 29, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K842123
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.