510(k) Report

FDA product code · Microbiology

Campylobacter Spp.

LQPClass I21 CFR 866.3110510(k) required12 decisions since 19861 recall

12 FDA decisions since 1986. 510(k) reviews decided 2021–2025 took a median of 235 days (half between 220 and 251). 1 recall names this code; it is not Class I. The most-cited predicate is K191456, 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, microbiology panel

Twenty years of LQP 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 · LQP

2in 2021

2009: 22018: 22019: 22021: 2
2007high 2 (2009) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · LQP

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

Recalls per year · LQP

No recall names LQP since 2007.

Adverse event reports per year · LQP

No MAUDE report names LQP since 2007.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20070—00
20080—00
20092—00
20100—00
20110—00
20120—00
20130—00
20140—00
20150—00
20160—00
20170—00
20182—00
20192—00
20200—00
20212—00
20220—00
20230—00
20240—00
20250—00
20260—0—
FIG. 1 — LQP by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in LQP? 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 866.3110.