510(k) K902443 ยท CEP Radioimmunoassay, Luteinizing Hormone
LUMATAG(TM) LH DIAGNOSTIC KIT
| Applicant | London Diagnostics, Inc., Eden Prairie MN, US |
| Decision | Substantially Equivalent, Aug 2, 1990 |
| Received | Jun 1, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K902443
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.