510(k) K920160 ยท CEP Radioimmunoassay, Luteinizing Hormone
LH GEN III SELF-TEST/CONCEIVE
| Applicant | Quidel Corp., San Diego CA, US |
| Decision | Substantially Equivalent, Mar 11, 1992 |
| Received | Jan 14, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K920160
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.