510(k) K820039 ยท CFT Radioimmunoassay, Prolactin (Lactogen)
LEECO PRL-QUANT DIAGNOSTIC TEST KIT
| Applicant | Leeco Diagnostics, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Jan 22, 1982 |
| Received | Jan 7, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K820039
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.