510(k) K821711 ยท DSI Detector And Alarm, Arrhythmia
CARDIO TEHCHANALYZER
| Applicant | Cardio Technology , Ltd., Mchenry IL, US |
| Decision | Substantially Equivalent, Oct 4, 1982 |
| Received | Jun 9, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K821711
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.