510(k) K895560 ยท LCX Kit, Test, Pregnancy, Hcg, Over The Counter
MODIFIED HOMECLINIC PREGNANCY TEST
| Applicant | Vanguard Biomedical Corp., San Diego CA, US |
| Decision | Substantially Equivalent, Nov 13, 1989 |
| Received | Sep 6, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K895560
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.