LGA — Device, Oxidase Test For Gonorrhea Class III

FDA Device Classification

FDA product code LGA covers "Device, Oxidase Test For Gonorrhea", a Class III medical device regulated under 21 CFR 866.2420. Submissions are reviewed by the Microbiology panel.

Classification Details

Product Code
LGA
Device Class
Class III
Regulation Number
866.2420
Submission Type
Review Panel
MI
Medical Specialty
Microbiology
Implant
No