510(k) K931678 ยท HMC Monitor, Eye Movement, Diagnostic
ORTHOMET LHMC FEMORAL STEM
| Applicant | Orthomet, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Oct 14, 1994 |
| Received | Apr 6, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K931678
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.