510(k) Report

FDA product code · General hospital

Cabinet, Ethylene-Oxide Gas Aerator

FLIClass II21 CFR 880.6100510(k) required8 decisions since 19770 recalls

8 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, general hospital panel

Twenty years of FLI 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 · FLI

FDA has decided no FLI device since 2007.

Median 510(k) review, days · FLI

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

Recalls per year · FLI

No recall names FLI since 2007.

Adverse event reports per year · FLI

1in 2012

2011: 12012: 1
2007high 1 (2011) · low 0 (2007)2025

MAUDE reports naming product code FLI, 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—00
20090—00
20100—00
20110—01
20120—01
20130—00
20140—00
20150—00
20160—00
20170—00
20180—00
20190—00
20200—00
20210—00
20220—00
20230—00
20240—00
20250—00
20260—0—
FIG. 1 — FLI by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in FLI? 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