510(k) K864149 ยท DSI Detector And Alarm, Arrhythmia
Q-SCAN II AND Q-SCAN III
| Applicant | Quinton, Inc., Seattle WA, US |
| Decision | Substantially Equivalent, Dec 10, 1986 |
| Received | Oct 22, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K864149
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.