510(k) K050094 ยท LHD Device, Fertility Diagnostic, Proceptive
LADY COMP USA
| Applicant | Lady Comp USA, Jeffersonville IN, US |
| Decision | Substantially Equivalent, Apr 20, 2006 |
| Received | Jan 14, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K050094
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.