510(k) K895094 ยท CEP Radioimmunoassay, Luteinizing Hormone
TANDEM-E LH IMMUNOENZYMETRIC ASSAY KIT
| Applicant | Hybritech, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Oct 31, 1989 |
| Received | Aug 14, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K895094
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.