510(k) Report

FDA product code · Pathology

Immunohistochemistry Assay, Antibody, Ki-67

QQTClass IIIPMA required1 decision since 20210 recalls

1 FDA decision since 2021. No recall names this code.

The Ki-67 antibody is a qualitative immunohistochemical antibody intended to identify Ki-67 protein expression in human clinical tissue specimens. The KI-67 antibody is indicated as an aid in identifying patients eligible for treatment with specific FDA approved therapeutic drugs.

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, pathology panel

Twenty years of QQT 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 · QQT

1in 2025

2021: 12024: 12025: 12026 (partial year): 1
2007high 1 (2021) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · QQT

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

Recalls per year · QQT

No recall names QQT since 2007.

Adverse event reports per year · QQT

No MAUDE report names QQT since 2007.

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
20150—00
20160—00
20170—00
20180—00
20190—00
20200—00
20211—00
20220—00
20230—00
20241—00
20251—00
20261—0—
FIG. 1 — QQT by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in QQT? A 510(k) Report ranks candidate predicates in this code by lineage, citations and recall history, with the review-time outlook.

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