510(k) Report

FDA product code · Microbiology

System, Transport, Aerobic

JTWClass I21 CFR 866.2900510(k) required43 decisions since 19766 recalls

43 FDA decisions since 1976. 6 recalls name this code, 0 of them Class I. The most-cited predicate is K061301, 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 JTW 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 · JTW

1in 2012

2012: 1
2007high 1 (2012) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · JTW

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

Recalls per year · JTW

1in 2022

2009: 12018: 42022: 1
2007high 4 (2018) · low 0 (2007)2026

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

Adverse event reports per year · JTW

36in 2025

2011: 22012: 22013: 12014: 32015: 22016: 22017: 142018: 322019: 82020: 122021: 72022: 52023: 222024: 372025: 36
2007high 37 (2024) · low 0 (2007)2025

MAUDE reports naming product code JTW, 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—10
20100—00
20110—02
20121—02
20130—01
20140—03
20150—02
20160—02
20170—014
20180—432
20190—08
20200—012
20210—07
20220—15
20230—022
20240—037
20250—036
20260—0—
FIG. 1 — JTW by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in JTW? 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 866.2900.