510(k) K852801 ยท LHD Device, Fertility Diagnostic, Proceptive
BIOCHRON FERTILITY INDICATOR
| Applicant | Fertil-A-Chron, Inc., Hauppauge NY, US |
| Decision | Substantially Equivalent, Sep 19, 1985 |
| Received | Jul 1, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K852801
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.