510(k) K880018 ยท IKK System, Isokinetic Testing And Evaluation
LIDO(TM) WORKSET
| Applicant | Loredan Biomedical, Inc., Davis CA, US |
| Decision | Substantially Equivalent, Feb 26, 1988 |
| Received | Jan 5, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880018
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.