510(k) K803282 ยท DSI Detector And Alarm, Arrhythmia
GUARDIAN MONITOR (CARDIOVASCULAR)
| Applicant | Bd Becton Dickinson Vacutainer Systems Preanalytic, Washington DC, US |
| Decision | Substantially Equivalent, Feb 27, 1981 |
| Received | Dec 29, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K803282
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.