510(k) K780232 ยท FMQ Restraint, Protective
RESTRAINT, PROTECTIVE
| Applicant | Biomet, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Feb 21, 1978 |
| Received | Feb 9, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K780232
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.