GTD — Antisera, Fluorescent, All Globulins, Shigella Spp. Class II

FDA Device Classification

FDA product code GTD covers "Antisera, Fluorescent, All Globulins, Shigella Spp.", a Class II medical device regulated under 21 CFR 866.3660. Submissions are reviewed by the Microbiology panel.

Classification Details

Product Code
GTD
Device Class
Class II
Regulation Number
866.3660
Submission Type
Review Panel
MI
Medical Specialty
Microbiology
Implant
No