Cyberfluor, Inc.
Cyberfluor, Inc. holds FDA 510(k) medical device clearances, first cleared 1987, most recent 1992.
Top product codes for Cyberfluor, Inc.
Recent clearances by Cyberfluor, Inc.
- K923410 — FIAGEN PROGESTERONE
- K905656 — FLAGEN TRIIODOTHYRONINE (T3) ASSAY
- K904539 — FLAGEN TM FREE T4
- K900621 — FIAGEN(TM) HLH.S
- K895186 — FIAGEN T3 UPTAKE CATALOGUE #101-402
- K895396 — CYBERFLUOR FIAGEN TSH
- K884707 — FIAGEN DIGOXIN TIME-RESOLVED FLUOROIMMUNOASSAY KIT
- K884708 — FIAGEN HFSH TIME-RESOLVED FLUOROIMMUNOASSAY KIT
- K884201 — FIAGEN TBG TIME-RESOLVED FLUOROIMMUNOASSAY KIT
- K883182 — FIAGEN RUBELLA IGG
- K882823 — FIAGEN HGH FLUOROIMMUNOASSAY KIT
- K882822 — FIAGEN FERRITIN
- K874623 — FIAGEN(TM) THYROXINE (T4), CATALOGUE #101-101
- K874621 — FIAGEN(TM) PROLACTIN CATALOGUE NUMBER: 102-201
- K874624 — FIAGEN(TM) HLH CATALOGUE NUMBER: 102-301
- K874622 — FIAGEN(TM) HTSH CATALOGUE NUMBER: 101-301
- K872803 — CYBERFLUOR 615 IMMUNOANALYZER
Data sourced from openFDA. This site is unofficial and independent of the FDA.