510(k) K902141 ยท FSA Lift, Patient, Non-Ac-Powered
ANOLIFT - PORTABLE & ANOLIFT - GANTRY
| Applicant | Anodyne Corp., Brighton MI, US |
| Decision | Substantially Equivalent, Sep 12, 1990 |
| Received | May 15, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K902141
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.