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GFE — Brush, Dermabrasion, Powered Class I

FDA Device Classification

Classification Details

Product Code
GFE
Device Class
Class I
Regulation Number
878.4820
Submission Type
Review Panel
SU
Medical Specialty
General, Plastic Surgery
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K963204aesthetic lasersDMS-1000C DERMOABRADERDecember 9, 1996
K905046aaron medical industriesDERMABRADERDecember 19, 1990