510(k) K881676 ยท IKK System, Isokinetic Testing And Evaluation
LINEAR LIFT DEVICE
| Applicant | Cybex, Ronkonkoma NY, US |
| Decision | Substantially Equivalent, Apr 25, 1990 |
| Received | Apr 19, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881676
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.