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

Chair, Surgical, Ac-Powered

21 CFR 878.4960 / General, Plastic Surgery
FDA source (opens on fda.gov)

GBB is the FDA product code for Chair, Surgical, Ac-Powered, a class I device type, regulated under 21 CFR 878.4960. As of , FDA records hold 8 510(k) clearances under this code, the most recent dated , and one recall.

Classification record

Product code
GBB
Device name
Chair, Surgical, Ac-Powered
Regulation
21 CFR 878.4960
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
8
Ingested recalls
1

Clearances, product code GBB

By decision year
8 clearances under product code GBB with a decision year between 1982 and 1996, 1982 the highest year at 4.
Show the numbers
510(k) clearances under FDA product code GBB by decision year
YearClearances
19824
19832
19891
19961

Applicants with the most clearances

Product code GBB
Applicants holding the most 510(k) clearances under product code GBB
ApplicantClearances
Kelleher Corp.3
Arthro-Medic, Inc.1
Medlog GmbH Marketing Services1
Midmark Corp1
Storz Instrument Co.1
Tenet Medical Engineering1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 44 companies shown, in name order