510(k) K023037 ยท LCX Kit, Test, Pregnancy, Hcg, Over The Counter
MID STREAM PREGNANCY TEST
| Applicant | Advanced Diagnostics, Inc., So. Plainfield NJ, US |
| Decision | Substantially Equivalent, Apr 9, 2003 |
| Received | Sep 12, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K023037
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.