510(k) K803001 ยท CDZ Radioimmunoassay, Testosterones And Dihydrotestosterone
LEECO TESTO-QUANT DIAGNOSTIC KIT
| Applicant | Leeco Diagnostics, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Jan 2, 1981 |
| Received | Nov 25, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K803001
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.