JLD — Chromatographic, Cystine Class I

FDA Device Classification

FDA product code JLD covers "Chromatographic, Cystine", a Class I medical device regulated under 21 CFR 862.1240. Submissions are reviewed by the Clinical Chemistry panel.

Classification Details

Product Code
JLD
Device Class
Class I
Regulation Number
862.1240
Submission Type
Review Panel
CH
Medical Specialty
Clinical Chemistry
Implant
No