510(k) K901969 ยท KMI Monitor, Bed Patient
ALERT BED ALARM SYSTEM
| Applicant | Alertronics, Inc., Tulsa OK, US |
| Decision | Substantially Equivalent, Sep 12, 1990 |
| Received | May 1, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K901969
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.