510(k) K820340 ยท KHQ Radioassay, Triiodothyronine Uptake
T3 UPTAKE-SQUIBB DIAGNOSTIC KIT
| Applicant | E. R. Squibb & Sons, Inc., New York NY, US |
| Decision | Substantially Equivalent, Mar 4, 1982 |
| Received | Feb 8, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K820340
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.