510(k) K863999 ยท LCX Kit, Test, Pregnancy, Hcg, Over The Counter
VIS-CUBE PREGNANCY HOME TEST,CAT. # JPL-042
| Applicant | Leeco Diagnostics, Inc., Southfield MI, US |
| Decision | Substantially Equivalent, Jan 9, 1987 |
| Received | Oct 14, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K863999
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.