DKS — Plate, Silica Gel, Tlc Class I

FDA Device Classification

FDA product code DKS covers "Plate, Silica Gel, Tlc", a Class I medical device regulated under 21 CFR 862.2270. Submissions are reviewed by the Clinical Chemistry panel.

Classification Details

Product Code
DKS
Device Class
Class I
Regulation Number
862.2270
Submission Type
Review Panel
TX
Medical Specialty
Clinical Chemistry
Implant
No