510(k) Report

FDA product code · Gastroenterology and urology

Enzyme Packed Cartridge

PLQClass II21 CFR 876.5985510(k) required8 decisions since 20150 recalls

8 FDA decisions since 2015. 510(k) reviews decided 2021–2025 took a median of 96 days (half between 82 and 108). No recall names this code. The most-cited predicate is DEN150001, named by 3 later devices.

Hydrolyze fats in enteral formula.

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 PLQ 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 · PLQ

2in 2025

2015: 12016: 12017: 12019: 12023: 22025: 2
2007high 2 (2023) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · PLQ

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

Recalls per year · PLQ

No recall names PLQ since 2007.

Adverse event reports per year · PLQ

2in 2025

2018: 12019: 32020: 42021: 12024: 32025: 2
2007high 4 (2020) · low 0 (2007)2025

MAUDE reports naming product code PLQ, 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—00
20120—00
20130—00
20140—00
20151—00
20161—00
20171—00
20180—01
20191—03
20200—04
20210—01
20220—00
20232—00
20240—03
20252—02
20260—0—
FIG. 1 — PLQ by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in PLQ? 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