510(k) K041039 ยท POV Semen Analysis Device
FERTELL MALE FERTILITY TEST
| Applicant | Genosis , Ltd., Washington DC, US |
| Decision | Substantially Equivalent, Jul 20, 2004 |
| Received | Apr 22, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K041039
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.