# Cyberfluor, Inc.

- Location (FDA's records): Ontario M5t 1x4, CA
- FDA decisions: 17 (1987–1992): 17 510(k) clearances
- Product codes: CEP (2), JLW (2), CGJ (1), CFL (1), CFT (1), JLS (1), CDP (1), DFL (1), KHO (1), LFX (1), KHQ (1), CEE (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K923410: Fiagen Progesterone (Dec 3, 1992)
- K905656: Flagen Triiodothyronine (T3) Assay (Jan 23, 1991)
- K904539: Flagen TM Free T4 (Nov 30, 1990)
- K900621: Fiagen (TM) HLH.S (Mar 1, 1990)
- K895186: Fiagen T3 Uptake Catalogue #101-402 (Nov 8, 1989)
- K895396: Cyberfluor Fiagen TSH (Oct 31, 1989)
- K884708: Fiagen HFSH Time-Resolved Fluoroimmunoassay Kit (Jan 17, 1989)
- K884707: Fiagen Digoxin Time-Resolved Fluoroimmunoassay Kit (Jan 17, 1989)

Source page: https://510kreport.com/company/cyberfluor