510(k) Report

FDA product code · Pathology

Microscope, Automated, Image Analysis, Operator Intervention

NOTClass II21 CFR 864.1860510(k) required13 decisions since 20031 recall

13 FDA decisions since 2003. 1 recall names this code; it is not Class I. The most-cited predicate is K032113, named by 4 later devices.

Automated microscopic immunohistochemistry image-analysis system to measure cell membrane intensity and pattern with operator intervention.

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 NOT 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 · NOT

1in 2014

2007: 22009: 22011: 12012: 22013: 12014: 12026 (partial year): 1
2007high 2 (2007) · low 0 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · NOT

Too few NOT 510(k)s in any year since 2007 to give a median.

Recalls per year · NOT

1in 2018

2018: 1
2007high 1 (2018) · low 0 (2007)2026

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

Adverse event reports per year · NOT

1in 2023

2014: 12015: 12023: 1
2007high 1 (2014) · low 0 (2007)2025

MAUDE reports naming product code NOT, 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
20072—00
20080—00
20092—00
20100—00
20111—00
20122—00
20131—00
20141—01
20150—01
20160—00
20170—00
20180—10
20190—00
20200—00
20210—00
20220—00
20230—01
20240—00
20250—00
20261—0—
FIG. 1 — NOT by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in NOT? 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 864.1860.