510(k) K020808 ยท NGE Test, Luteinizing Hormone (Lh), Over The Counter
FERTILITE OV
| Applicant | Pheromone Sciences Corp., Toronto, CA |
| Decision | Substantially Equivalent, Sep 23, 2002 |
| Received | Mar 12, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K020808
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.