510(k) K811792 ยท DSI Detector And Alarm, Arrhythmia
ARRYTHMIA PRINTER OPTION
| Applicant | American Edwards Laboratories, Mchenry IL, US |
| Decision | Substantially Equivalent, Jul 10, 1981 |
| Received | Jun 24, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K811792
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.