510(k) Report

FDA product code · Gastroenterology and urology

Connector, Tubing, Dialysate

FKYClass II21 CFR 876.5820510(k) required4 decisions since 19770 recalls

4 FDA decisions since 1977. No recall names this code.

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 FKY 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 · FKY

FDA has decided no FKY device since 2007.

Median 510(k) review, days · FKY

Too few FKY 510(k)s in any year since 2007 to give a median.

Recalls per year · FKY

No recall names FKY since 2007.

Adverse event reports per year · FKY

4in 2023

2008: 22023: 4
2007high 4 (2023) · low 0 (2007)2025

MAUDE reports naming product code FKY, 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—00
20080—02
20090—00
20100—00
20110—00
20120—00
20130—00
20140—00
20150—00
20160—00
20170—00
20180—00
20190—00
20200—00
20210—00
20220—00
20230—04
20240—00
20250—00
20260—0—
FIG. 1 — FKY by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in FKY? 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 876.5820.