510(k) K863929 ยท CEP Radioimmunoassay, Luteinizing Hormone
TERUMO SENSIBEAD(TM) EIA HLH KIT
| Applicant | Terumo Medical Corp., Elkton MD, US |
| Decision | Substantially Equivalent, Nov 13, 1986 |
| Received | Oct 8, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K863929
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.