510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
GEEClass I

Brush, Biopsy, General & Plastic Surgery

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

GEE is the FDA product code for Brush, Biopsy, General & Plastic Surgery, a class I device type, regulated under 21 CFR 878.4800. As of , FDA records hold 7 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
GEE
Device name
Brush, Biopsy, General & Plastic Surgery
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
7
Ingested recalls
0

Clearances, product code GEE

By decision year
7 clearances under product code GEE with a decision year between 1979 and 1985, 1982 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code GEE by decision year
YearClearances
19791
19801
19811
19822
19841
19851

Applicants with the most clearances

Product code GEE
Applicants holding the most 510(k) clearances under product code GEE
ApplicantClearances
American Endoscopy, Inc.1
Co-Medical, Inc.1
Johannah Medical Services, Inc.1
Medi-Spec1
Premier Dental Products Co1
Ursus Konsult AB1
Van-Tec, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 39 companies shown, in name order