510(k) K830808 ยท CDP Radioimmunoassay, Total Triiodothyronine
LEECO T3-RIA DIAGNOSTIC KIT
| Applicant | Leeco Diagnostics, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Apr 8, 1983 |
| Received | Mar 14, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K830808
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.