510(k) K081922 ยท JLX Radioimmunoassay, 17-Hydroxyprogesterone
AUTODELFIA NEONATAL 17A-OH-PROGESTERONE KIT
| Applicant | Wallac OY, Turku, FI |
| Decision | Substantially Equivalent, Apr 16, 2009 |
| Received | Jul 7, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K081922
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.