510(k) K822449 ยท LCX Kit, Test, Pregnancy, Hcg, Over The Counter
TPK 1980/1
| Applicant | Plantex USA, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Oct 27, 1982 |
| Received | Aug 16, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K822449
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.