GMB — Light, Wood'S, Fluorescence Class I

FDA Device Classification

FDA product code GMB covers "Light, Wood'S, Fluorescence", a Class I medical device regulated under 21 CFR 866.2600. Submissions are reviewed by the Microbiology panel.

Classification Details

Product Code
GMB
Device Class
Class I
Regulation Number
866.2600
Submission Type
Review Panel
MI
Medical Specialty
Microbiology
Implant
No