510(k) K915229 ยท POV Semen Analysis Device
SEMEN ANALYSIS KIT
| Applicant | Humagen Fertility Diagnostics, Inc., Charlottesville VA, US |
| Decision | Substantially Equivalent, Aug 30, 1994 |
| Received | Nov 20, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K915229
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.