DNX — Lead, Protoporphyrin Zinc Method, Fluorometric Class II

FDA Device Classification

FDA product code DNX covers "Lead, Protoporphyrin Zinc Method, Fluorometric", a Class II medical device regulated under 21 CFR 862.3550. Submissions are reviewed by the Clinical Toxicology panel.

Classification Details

Product Code
DNX
Device Class
Class II
Regulation Number
862.3550
Submission Type
Review Panel
TX
Medical Specialty
Clinical Toxicology
Implant
No