510(k) K882343 ยท CHP Radioimmunoassay, Estradiol
TERUMO SENSIBEAD(TM) EIA ESTRADIOL KIT
| Applicant | Terumo Medical Corp., Elkton MD, US |
| Decision | Substantially Equivalent, Jul 1, 1988 |
| Received | Jun 7, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K882343
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.