510(k) K883390 ยท KMI Monitor, Bed Patient
PMD SYSTEM-20
| Applicant | Datatek, Inc., Shreveport LA, US |
| Decision | Substantially Equivalent, Oct 25, 1988 |
| Received | Aug 9, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K883390
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.