510(k) Report

FDA product code · Clinical chemistry

Diazo (Colorimetric), Nitrite (Urinary, Non-Quant)

JMTClass I21 CFR 862.1510510(k) exempt13 decisions since 19842 recalls

FDA lists JMT as exempt from 510(k): a device of this type needs no clearance unless one of the limits in 21 CFR 862.9 applies, such as a new intended use or a different fundamental technology. 13 FDA decisions since 1984. 510(k) reviews decided 2021–2025 took a median of 119 days (half between 96 and 157). 2 recalls name this code, 0 of them Class I. The most-cited predicate is K100024, named by 1 later device.

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, clinical chemistry panel

Twenty years of JMT 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 · JMT

3in 2025

2011: 12017: 12025: 3
2007high 3 (2025) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · JMT

119in 2025

2025: 119 days median
2007high 119 (2025)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · JMT

2in 2023

2023: 2
2007high 2 (2023) · low 0 (2007)2026

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

Adverse event reports per year · JMT

2in 2020

2018: 12019: 32020: 2
2007high 3 (2019) · low 0 (2007)2025

MAUDE reports naming product code JMT, 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
20111—00
20120—00
20130—00
20140—00
20150—00
20160—00
20171—00
20180—01
20190—03
20200—02
20210—00
20220—00
20230—20
20240—00
2025311900
20260—0—
FIG. 1 — JMT by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in JMT? 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 862.1510.