510(k) K032002 ยท NGA Test, Follicle Stimulating Hormone (Fsh), Over The Counter
FERTELL FEMALE FERTILITY TEST
| Applicant | Genosis, Inc., Washington DC, US |
| Decision | Substantially Equivalent, Oct 30, 2003 |
| Received | Jun 27, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K032002
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.