510(k) K781911 ยท DSI Detector And Alarm, Arrhythmia
ECG ANALYZER, HIGH SPEED
| Applicant | Cardio-Dynamics Laboratories, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Nov 30, 1978 |
| Received | Nov 14, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K781911
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.