GPX — Antisera, Neutralizion, Reovirus 1-3 Class I

FDA Device Classification

FDA product code GPX covers "Antisera, Neutralizion, Reovirus 1-3", a Class I medical device regulated under 21 CFR 866.3470. Submissions are reviewed by the Microbiology panel.

Classification Details

Product Code
GPX
Device Class
Class I
Regulation Number
866.3470
Submission Type
Review Panel
MI
Medical Specialty
Microbiology
Implant
No