510(k) K050546 ยท LCX Kit, Test, Pregnancy, Hcg, Over The Counter
ACON +/- MIDSTREAM PREGNANCY TEST
| Applicant | ACON Laboratories, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, May 20, 2005 |
| Received | Mar 2, 2005 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K050546
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.