510(k) K820251 ยท CDP Radioimmunoassay, Total Triiodothyronine
T4 DIAGNOSTIC KIT
| Applicant | Diagnostic Reagents, Inc., Walker MI, US |
| Decision | Substantially Equivalent, May 5, 1982 |
| Received | Jan 29, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K820251
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.