GED — Brush, Dermabrasion, Manual Class I

FDA Device Classification

FDA product code GED covers "Brush, Dermabrasion, Manual", a Class I medical device regulated under 21 CFR 878.4800. Submissions are reviewed by the General, Plastic Surgery panel. At least 2 recent 510(k) clearances have been granted under this product code.

Classification Details

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

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K830259ritmedPROTET SOAP & WASH MITTMay 9, 1983
K821801bel-medNORSEN DEBRIDERJuly 28, 1982