FBQClass II

Trocar, Gastro-Urology

21 CFR 876.5090 / Gastroenterology, Urology

FBQ is the FDA product code for Trocar, Gastro-Urology, a class II device type, regulated under 21 CFR 876.5090. As of 2026-09-10, FDA records hold 9 510(k) clearances under this code, the most recent dated 2001-08-09, and 25 recalls.

Classification record

Product code: FBQ
Device name: Trocar, Gastro-Urology
Regulation: 21 CFR 876.5090
Device class: Class II
Review panel: Gastroenterology, Urology
Submission type: 510(k) exempt
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: No
Ingested clearances: 9
Ingested recalls: 25

Clearances, product code FBQ

By decision year

9 clearances under product code FBQ with a decision year between 1984 and 2001, 1994 the highest year at 3.

Show the numbers

510(k) clearances under FDA product code FBQ by decision year
Year	Clearances
1984	1
1990	1
1991	1
1993	1
1994	3
1998	1
2001	1

Applicants with the most clearances

Product code FBQ

Applicants holding the most 510(k) clearances under product code FBQ
Applicant	Clearances
Gabris Surgical Corp.	2
United States Surgical, A Division of Tyco Healthc	2
Aesculap Inc	1
Endoscopic Concepts, Inc.	1
Endotherapeutics	1
Gibbons Surgical Corp.	1
L.A.S.E.R., Inc.	1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 30 companies shown, in name order