510(k) K850056 ยท JLS Radioimmunoassay, Progesterone
LEECO PROGESTERONE-QUANT DIAGNOSTIC TEST KIT
| Applicant | Leeco Diagnostics, Inc., Southfield MI, US |
| Decision | Substantially Equivalent, Feb 6, 1985 |
| Received | Jan 8, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K850056
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.