510(k) K780240 ยท LCX Kit, Test, Pregnancy, Hcg, Over The Counter
PREDICTOR
| Applicant | Organon, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Feb 27, 1978 |
| Received | Feb 13, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K780240
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.