510(k) K910830 ยท FRZ Device, Patient Transfer, Powered
INVALIFT
| Applicant | American Invalift Corp., White Plains NY, US |
| Decision | Substantially Equivalent, Jun 9, 1992 |
| Received | Feb 27, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K910830
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.