510(k) K872131 ยท CEP Radioimmunoassay, Luteinizing Hormone
TANDEMR M-PAK LH IMMUNOENZYMETRIC ASSAY
| Applicant | Hybritech, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Aug 25, 1987 |
| Received | Jun 4, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K872131
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.