510(k) K834474 ยท LCX Kit, Test, Pregnancy, Hcg, Over The Counter
H.P.T. HOME PREG. TEST KIT & A.P.T.
| Applicant | Biomedical Research & Development Laboratories, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Sep 28, 1984 |
| Received | Dec 20, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K834474
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.