510(k) K883826 ยท LCX Kit, Test, Pregnancy, Hcg, Over The Counter
HOME CLINIC PREGNANCY TEST
| Applicant | Vanguard Biomedical Corp., San Diego CA, US |
| Decision | Substantially Equivalent, Nov 29, 1988 |
| Received | Sep 9, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K883826
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.