510(k) K841083 ยท DSI Detector And Alarm, Arrhythmia
QUIKPAGE ARRHYTHMIA REPORT GENERATOR
| Applicant | Agilent Technologies, Camarillo CA, US |
| Decision | Substantially Equivalent, Feb 7, 1985 |
| Received | Mar 13, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K841083
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.