510(k) K962355 ยท CDP Radioimmunoassay, Total Triiodothyronine
FREE TRIIODOTHYRONINE(FT3) ASSAY FOR THE TECHNICON IMMUNO 1 SYSTEM (IN-VITRO DIAGNOSTIC SYSTEM)
| Applicant | Bayer Corp., Tarrytown NY, US |
| Decision | Substantially Equivalent, Jul 12, 1996 |
| Received | Jun 18, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K962355
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.