GRG — Antiserum, Hai, Rubeola Class I

FDA Device Classification

FDA product code GRG covers "Antiserum, Hai, Rubeola", a Class I medical device regulated under 21 CFR 866.3520. Submissions are reviewed by the Microbiology panel.

Classification Details

Product Code
GRG
Device Class
Class I
Regulation Number
866.3520
Submission Type
Review Panel
MI
Medical Specialty
Microbiology
Implant
No