510(k) K882978 ยท DSI Detector And Alarm, Arrhythmia
Q4000 OPTION FOR Q4000
| Applicant | Quinton, Inc., Seattle WA, US |
| Decision | Substantially Equivalent, Nov 1, 1988 |
| Received | Jul 15, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K882978
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.