510(k) K801903 ยท DSI Detector And Alarm, Arrhythmia
SERIES 4000 STRESS & EXERCISE SYSTEM
| Applicant | Instruments For Cardiac Research, Walker MI, US |
| Decision | Substantially Equivalent, Mar 11, 1981 |
| Received | Aug 11, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K801903
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.