510(k) K884216 ยท DSI Detector And Alarm, Arrhythmia
506 NON-INVASIVE VITAL SIGNS MONITOR
| Applicant | Criticare Systems, Inc., Milwaukee WI, US |
| Decision | Substantially Equivalent, Mar 16, 1989 |
| Received | Oct 6, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K884216
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.