510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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GEDClass I

Brush, Dermabrasion, Manual

21 CFR 878.4800 / General, Plastic Surgery
FDA source (opens on fda.gov)

GED is the FDA product code for Brush, Dermabrasion, Manual, a class I device type, regulated under 21 CFR 878.4800. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
GED
Device name
Brush, Dermabrasion, Manual
Regulation
21 CFR 878.4800
Device class
Class I
Review panel
General, Plastic Surgery
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
2
Ingested recalls
0

Clearances, product code GED

By decision year
2 clearances under product code GED with a decision year between 1982 and 1983, 1982 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code GED by decision year
YearClearances
19821
19831

Applicants with the most clearances

Product code GED
Applicants holding the most 510(k) clearances under product code GED
ApplicantClearances
Bel-Med, Inc1
Ritmed, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 47 companies shown, in name order