510(k) K860003 ยท CDZ Radioimmunoassay, Testosterones And Dihydrotestosterone
LEECO TESTOSTERONE DIAGNOSTIC KIT
| Applicant | Leeco Diagnostics, Inc., Southfield MI, US |
| Decision | Substantially Equivalent, Mar 17, 1986 |
| Received | Jan 2, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K860003
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.