DGW — System, Test, Hypersensitivity Pneumonitis Class II

FDA Device Classification

FDA product code DGW covers "System, Test, Hypersensitivity Pneumonitis", a Class II medical device regulated under 21 CFR 866.5500. Submissions are reviewed by the Immunology panel.

Classification Details

Product Code
DGW
Device Class
Class II
Regulation Number
866.5500
Submission Type
Review Panel
IM
Medical Specialty
Immunology
Implant
No