510(k) K951360 ยท CHP Radioimmunoassay, Estradiol
ESTRADIOL ASSAY FOR THE TECHNICON IMMUNO 1 SYSTEM IN-VITRO DIAGNOSTIC SYSTEM
| Applicant | Bayer Corp., Tarrytown NY, US |
| Decision | Substantially Equivalent, May 2, 1995 |
| Received | Mar 27, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K951360
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.