JLL — Tubeless Analysis, Gastric Acidity Class I

FDA Device Classification

FDA product code JLL covers "Tubeless Analysis, Gastric Acidity", a Class I medical device regulated under 21 CFR 862.1320. Submissions are reviewed by the Clinical Chemistry panel.

Classification Details

Product Code
JLL
Device Class
Class I
Regulation Number
862.1320
Submission Type
Review Panel
CH
Medical Specialty
Clinical Chemistry
Implant
No