510(k) K920920 ยท CEP Radioimmunoassay, Luteinizing Hormone
ELISA TUBE LH TEST KIT
| Applicant | Bio Clinic Co., St. Louis MI, US |
| Decision | Substantially Equivalent, Apr 8, 1992 |
| Received | Feb 28, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K920920
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.