510(k) K833466 ยท LCX Kit, Test, Pregnancy, Hcg, Over The Counter
EARLY PREGNANCY DETECTION TEST KIT
| Applicant | Quidel Corp., Washington DC, US |
| Decision | Substantially Equivalent, Nov 25, 1983 |
| Received | Oct 6, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K833466
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.