510(k) K983090 ยท LCX Kit, Test, Pregnancy, Hcg, Over The Counter
ACON MIDSTREAM PREGNANCY TEST
| Applicant | ACON Laboratories, Inc., Allentown PA, US |
| Decision | Substantially Equivalent, Nov 18, 1998 |
| Received | Sep 3, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K983090
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.