Liqui-Sera Anticonvulsants Controls

No FDA recalls found in the data synced 10 Oct 2026.

510(k) Number

K831278 ↗

FDA Product Code

DIF

Device Class

Class I

Regulation

21 CFR Part 862.3280

Advisory Committee

Clinical Toxicology

FDA Decision

SESE Substantially Equivalent

• Liqui-Sera Serum Alcohol Controls

  Class I

  FDA 510(k) K881430 Active Cleared 8 Jul 1988

• Liqui-Sera Chemistry Controls (Comprehensive)

  Class I

  FDA 510(k) K853906 Active Cleared 4 Oct 1985

• Liqui-Ura Chemistry Urine Controls

  Class I

  FDA 510(k) K840618 Active Cleared 4 Apr 1984

• Liqui-Sera Spinal Fluid Control

  Class I

  FDA 510(k) K874459 Active Cleared 29 Dec 1987

• Liqui-Heme Hemoglobin Calibrators

  Class II

  FDA 510(k) K842668 Active Cleared 5 Mar 1985

• Liqui-Sera Tdm Calibrators

  Class II

  FDA 510(k) K834398 Active Cleared 3 Feb 1984

See all devices from Biodiagnostic Intl →