510(k) K870999 ยท LHD Device, Fertility Diagnostic, Proceptive
GENDER CHOICE INFORMATION KIT, FEMALE AND MALE
| Applicant | Procare C/O Wiley, Rein & Fielding, Washington DC, US |
| Decision | Substantially Equivalent, Jul 14, 1987 |
| Received | Mar 11, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K870999
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.