JMI — Chromatographic, Histidine Class I

FDA Device Classification

FDA product code JMI covers "Chromatographic, Histidine", a Class I medical device regulated under 21 CFR 862.1375. Submissions are reviewed by the Clinical Chemistry panel.

Classification Details

Product Code
JMI
Device Class
Class I
Regulation Number
862.1375
Submission Type
Review Panel
CH
Medical Specialty
Clinical Chemistry
Implant
No