510(k) K952075 ยท JLS Radioimmunoassay, Progesterone
PROGESTERONE ASSAY FOR THE TECHNICON IMMUNO 1 SYSTEM IN-BITRO DIAGNOSTIC SYSTEM
| Applicant | Bayer Corp., Tarrytown NY, US |
| Decision | Substantially Equivalent, Jun 13, 1995 |
| Received | May 3, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K952075
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.