510(k) K912026 ยท JLX Radioimmunoassay, 17-Hydroxyprogesterone
DELFIA(R) 17 -OH-PROGESTERON KIT
| Applicant | Pharmacia Diagnostics, Inc., Columbia MD, US |
| Decision | Substantially Equivalent, Jun 25, 1991 |
| Received | May 7, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K912026
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.