DEK — Kappa, Rhodamine, Antigen, Antiserum, Control Class II

FDA Device Classification

FDA product code DEK covers "Kappa, Rhodamine, Antigen, Antiserum, Control", a Class II medical device regulated under 21 CFR 866.5550. Submissions are reviewed by the Immunology panel.

Classification Details

Product Code
DEK
Device Class
Class II
Regulation Number
866.5550
Submission Type
Review Panel
IM
Medical Specialty
Immunology
Implant
No