JNG — Radioimmunoassay, Pregnenolone Class I

FDA Device Classification

FDA product code JNG covers "Radioimmunoassay, Pregnenolone", a Class I medical device regulated under 21 CFR 862.1615. Submissions are reviewed by the Clinical Chemistry panel.

Classification Details

Product Code
JNG
Device Class
Class I
Regulation Number
862.1615
Submission Type
Review Panel
CH
Medical Specialty
Clinical Chemistry
Implant
No