510(k) K914859 ยท KMI Monitor, Bed Patient
BARTRONIX IN-BED ACTIVITY MONITOR
| Applicant | Bartronix, Fort Worth TX, US |
| Decision | Substantially Equivalent, Apr 13, 1992 |
| Received | Oct 29, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K914859
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.