510(k) K820438 ยท DSI Detector And Alarm, Arrhythmia
QUINTON Q2000 ETT MONITORING SYSTEM
| Applicant | Quinton, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Apr 29, 1982 |
| Received | Feb 17, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K820438
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.