LDB — U.V. Spectrometry, Carbamazepine Class II

FDA Device Classification

FDA product code LDB covers "U.V. Spectrometry, Carbamazepine", a Class II medical device regulated under 21 CFR 862.3645. Submissions are reviewed by the Clinical Toxicology panel.

Classification Details

Product Code
LDB
Device Class
Class II
Regulation Number
862.3645
Submission Type
Review Panel
TX
Medical Specialty
Clinical Toxicology
Implant
No