510(k) K881876 ยท LYH Arthrometer
DYNAMIC CRUCIATE TESTER
| Applicant | Dyonics, Inc., Andover MA, US |
| Decision | Substantially Equivalent, Nov 17, 1988 |
| Received | May 4, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881876
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.