510(k) Report

FDA product code · General hospital

Pad, Alcohol, Device Disinfectant

LKBClass U25 decisions since 19815 recalls

25 FDA decisions since 1981. 5 recalls name this code, 0 of them Class I. The most-cited predicate is K833182, named by 3 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, general hospital panel

Twenty years of LKB 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 · LKB

1in 2014

2012: 12013: 12014: 1
2007high 1 (2012) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · LKB

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

Recalls per year · LKB

5in 2011

2011: 5
2007high 5 (2011) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · LKB

14in 2025

2008: 12011: 62012: 32013: 32014: 62015: 12016: 72017: 432018: 212019: 372020: 392021: 402022: 92023: 292024: 112025: 14
2007high 43 (2017) · low 0 (2007)2025

MAUDE reports naming product code LKB, 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—01
20090—00
20100—00
20110—56
20121—03
20131—03
20141—06
20150—01
20160—07
20170—043
20180—021
20190—037
20200—039
20210—040
20220—09
20230—029
20240—011
20250—014
20260—0—
FIG. 1 — LKB by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in LKB? 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