510(k) K901330 ยท KMI Monitor, Bed Patient
THE MONITOR ELECTRONIC BED ALARM SYSTEM
| Applicant | The Monitor Corp., Dallas TX, US |
| Decision | Substantially Equivalent, Aug 30, 1990 |
| Received | Mar 22, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K901330
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.