510(k) Report

FDA product code · Gastroenterology and urology

Choledochoscope And Accessories, Flexible/Rigid

FBNClass II21 CFR 876.1500510(k) required43 decisions since 19774 recalls

43 FDA decisions since 1977. 510(k) reviews decided 2021–2025 took a median of 190 days (half between 162 and 244). 4 recalls name this code, 1 of them Class I. The most-cited predicate is K060269, named by 7 later devices.

to examine and perform procedures within the bile ducts. For reusable, flexible endoscopes in this product code, validated reprocessing instructions and reprocessing validation data must be included in a 510(k) submission (82 FR 26807, available at https://www.gpo.gov/fdsys/pkg/FR-2017-06-09/pdf/2017-12007.pdf).

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026 Download the data (CSV)

FIG. A — Illustration, gastroenterology and urology panel

Twenty years of FBN at a glance: how often FDA decides these devices, how long 510(k) reviews take, how often they are recalled, and how many adverse event reports name the code.

FDA decisions per year · FBN

3in 2025

2008: 32010: 12012: 12015: 12016: 12018: 12019: 12020: 12023: 42024: 22025: 32026 (partial year): 3
2007high 4 (2023) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · FBN

150in 2025

2008: 64 days median2023: 215 days median2025: 150 days median2026 (partial year): 175 days median
2007high 215 (2023) · low 64 (2008)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · FBN

1in 2024

2020: 12023: 12024: 1, 1 Class I2026 (partial year): 1
2007high 1 (2020) · low 0 (2007)2026

Class I (1 since 2007) Class II/III not classified

Adverse event reports per year · FBN

118in 2025

2007: 12008: 52009: 42010: 22011: 22013: 22014: 22015: 22016: 1682017: 2242018: 6392019: 1052020: 1732021: 1582022: 2832023: 1052024: 1072025: 118
2007high 639 (2018) · low 0 (2012)2025

MAUDE reports naming product code FBN, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20070—01
200836405
20090—04
20101—02
20110—02
20121—00
20130—02
20140—02
20151—02
20161—0168
20170—0224
20181—0639
20191—0105
20201—1173
20210—0158
20220—0283
202342151105
20242—1 (1)107
202531500118
202631751—
FIG. 1 — FBN by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in FBN? A 510(k) Report ranks candidate predicates in this code by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Related product codes

Other codes under 21 CFR 876.1500.