QBK

Meprobamate Test System

Product code

QBK

Device name

Meprobamate Test System

Device class

Class 2

21 CFR

21 CFR 862.3590

Medical specialty

Clinical Toxicology

Marketing pathway

510(K)

Flag

Third-party review eligible

510(k) clearances (all years, FDA)

2 (all years; only the last 3 years are listed here)

FDA classification definition

A meprobamate test system is a device intended to measure meprobamate in human specimens. Measurements obtained by this device are used to detect the presence of meprobamate to diagnose the use or overdose of meprobamate or structurally-related drug compounds (e.g., prodrugs).

Definition text from the FDA device classification database (U.S. federal government work, public domain).