DLX — Hemagglutination Inhibition, Barbiturate Class II

FDA Device Classification

FDA product code DLX covers "Hemagglutination Inhibition, Barbiturate", a Class II medical device regulated under 21 CFR 862.3150. Submissions are reviewed by the Clinical Toxicology panel.

Classification Details

Product Code
DLX
Device Class
Class II
Regulation Number
862.3150
Submission Type
Review Panel
TX
Medical Specialty
Clinical Toxicology
Implant
No