510(k) K910808 ยท DSI Detector And Alarm, Arrhythmia
Q-SMART HOLTER SYSTEMS
| Applicant | Quinton, Inc., Seattle WA, US |
| Decision | Substantially Equivalent, Jul 17, 1991 |
| Received | Feb 26, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K910808
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.