Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Cyberfluor with 17 510(k) clearances. The most recent is a 510(k) clearance dated Dec 3, 1992: FIAGEN PROGESTERONE.
| Date | Record | Source |
|---|---|---|
| Dec 3, 1992 | FIAGEN PROGESTERONEK923410 · JLS | 510(k) clearances |
| Jan 23, 1991 | FLAGEN TRIIODOTHYRONINE (T3) ASSAYK905656 · CDP | 510(k) clearances |
| Nov 30, 1990 | FLAGEN TM FREE T4K904539 · CEC | 510(k) clearances |
| Mar 1, 1990 | FIAGEN(TM) HLH.SK900621 · CEP | 510(k) clearances |
| Nov 8, 1989 | FIAGEN T3 UPTAKE CATALOGUE #101-402K895186 · KHQ | 510(k) clearances |
| Oct 31, 1989 | CYBERFLUOR FIAGEN TSHK895396 · JLW | 510(k) clearances |
| Jan 17, 1989 | FIAGEN HFSH TIME-RESOLVED FLUOROIMMUNOASSAY KITK884708 · CGJ | 510(k) clearances |
| Jan 17, 1989 | FIAGEN DIGOXIN TIME-RESOLVED FLUOROIMMUNOASSAY KITK884707 · LCS | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
