CDE — Chromatographic Separation/Zimmerman, 17-Ketosteroids Class I

FDA Device Classification

FDA product code CDE covers "Chromatographic Separation/Zimmerman, 17-Ketosteroids", a Class I medical device regulated under 21 CFR 862.1430. Submissions are reviewed by the Clinical Chemistry panel.

Classification Details

Product Code
CDE
Device Class
Class I
Regulation Number
862.1430
Submission Type
Review Panel
CH
Medical Specialty
Clinical Chemistry
Implant
No