GAI — Stripper, Vein, Reusable Class I

FDA Device Classification

FDA product code GAI covers "Stripper, Vein, Reusable", a Class I medical device regulated under 21 CFR 878.4800. Submissions are reviewed by the General, Plastic Surgery panel.

Classification Details

Product Code
GAI
Device Class
Class I
Regulation Number
878.4800
Submission Type
Review Panel
SU
Medical Specialty
General, Plastic Surgery
Implant
No