Randox Laboratories, Ltd.
Randox Laboratories, Ltd. holds FDA 510(k) medical device clearances, first cleared 1992, most recent 2025, with 79 FDA device recalls on record.
Clearances by Randox Laboratories, Ltd. — page 2
101–116 of 116- K951221 — TOTAL CO2
- K951223 — CK-MB (NAC-ACT)
- K954447 — C-REACTIVE PROTEIN LATEX KIT
- K950382 — APOLIPOPROTEIN B IMMUNOTURBIDIEMETRIC KIT
- K950383 — APOLIPOPROTEIN A-I IMMUNOTURBIDIMETRIC KIT
- K953212 — C-REACTIVE PROTEIN IMMUNOTURBIDIMETRIC KIT & CRP CALIBRATOR
- K942458 — PRECISION-MULTI-SERA - HUMAN - NORMAL AND ELEVATED
- K923504 — CHOLESTEROL ENZYMATIC ENDPOINT
- K923506 — UREA KIT
- K923508 — TRIGLYCERIDES GPO-PAP
- K923503 — URIC ACID ENZYMATIC COLORIMERIC KIT
- K923507 — ALKALINE PHOSPHATASE KIT
- K923509 — GAMMA-GT
- K923505 — AST (GOT) - ASPARTATE AMINOTRANSFERASE
- K923510 — ALT (GPT) - ALANINE AMINOTRANSFERASE
- K923511 — CK-NAC ACTIVATED KIT
Data sourced from openFDA. This site is unofficial and independent of the FDA.