510(k) Report

FDA product code · Gastroenterology and urology

Filter, Blood, Dialysis

FKJClass II21 CFR 876.5820510(k) required5 decisions since 19770 recalls

5 FDA decisions since 1977. No recall names this code. The most-cited predicate is K901734, named by 2 later devices.

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 FKJ 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 · FKJ

1so far in 2026, the most since 2007

2026 (partial year): 1
2007high 1 (2026) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · FKJ

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

Recalls per year · FKJ

No recall names FKJ since 2007.

Adverse event reports per year · FKJ

1in 2025

2007: 72008: 32009: 32010: 42013: 52015: 22016: 482017: 112025: 1
2007high 48 (2016) · low 0 (2011)2025

MAUDE reports naming product code FKJ, 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—07
20080—03
20090—03
20100—04
20110—00
20120—00
20130—05
20140—00
20150—02
20160—048
20170—011
20180—00
20190—00
20200—00
20210—00
20220—00
20230—00
20240—00
20250—01
20261—0—
FIG. 1 — FKJ by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in FKJ? 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.