510(k) K854058 ยท FNG Lift, Patient, Ac-Powered
PK-AC POWERED PATIENT MANUPULATING DEVICE
| Applicant | Mannesmann Demag Corp., Solon OH, US |
| Decision | Substantially Equivalent, Feb 25, 1986 |
| Received | Oct 3, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K854058
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.