510(k) K974821 ยท LCX Kit, Test, Pregnancy, Hcg, Over The Counter
BLUETEST(R) PREGNANCY TEST, RAPIDVUE(R) PREGNANCY TEST
| Applicant | Quidel Corp., San Diego CA, US |
| Decision | Substantially Equivalent, Jan 26, 1998 |
| Received | Dec 23, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K974821
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.