510(k) K880069 ยท LCX Kit, Test, Pregnancy, Hcg, Over The Counter
LEECO PREGNASTICK (EIA) CATALOG #003
| Applicant | Leeco Diagnostics, Inc., Southfield MI, US |
| Decision | Substantially Equivalent, Feb 11, 1988 |
| Received | Jan 11, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880069
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.