510(k) K002726 ยท LHD Device, Fertility Diagnostic, Proceptive
TCOYF FERTILITY SOFTWARE VERSION 1.0
| Applicant | Ovusoft, LLC, Hampton VA, US |
| Decision | Substantially Equivalent, Apr 6, 2001 |
| Received | Aug 31, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K002726
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.