510(k) K050919 ยท DSI Detector And Alarm, Arrhythmia
LIFEGARD II FAMILY MULTI-FUNCTION PATIENT MONITOR, MODELS AN4320, AN4320P, AN4321P, AN4322P & AN3423P
| Applicant | Analogic Corp., Peabody MA, US |
| Decision | Substantially Equivalent, Jun 14, 2005 |
| Received | Apr 12, 2005 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K050919
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.