510(k) K023638 ยท LCX Kit, Test, Pregnancy, Hcg, Over The Counter
CASSETTE/URINE HCG
| Applicant | Ind Diagnostic, Inc., Delta, B.C., CA |
| Decision | Substantially Equivalent, Jan 3, 2003 |
| Received | Oct 30, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K023638
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.