510(k) K834397 ยท DSI Detector And Alarm, Arrhythmia
HOLTER CARDIOGRAPHY SYS 6201
| Applicant | Instruments For Cardiac Research, Mchenry IL, US |
| Decision | Substantially Equivalent, Apr 17, 1984 |
| Received | Dec 14, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K834397
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.