510(k) Report

FDA product code · Microbiology

Culture Media, Antimicrobial Susceptibility Test, Mueller Hinton Agar/Broth

JTZClass II21 CFR 866.1700510(k) required75 decisions since 19787 recalls

75 FDA decisions since 1978. 7 recalls name this code, 0 of them Class I. The most-cited predicate is K863821, named by 5 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 JTZ 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 · JTZ

1in 2014

2014: 12026 (partial year): 1
2007high 1 (2014) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · JTZ

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

Recalls per year · JTZ

1in 2025

2008: 12009: 22011: 12017: 12025: 1
2007high 2 (2009) · low 0 (2007)2026

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

Adverse event reports per year · JTZ

20in 2025

2008: 12011: 12021: 202022: 272023: 202024: 92025: 20
2007high 27 (2022) · low 0 (2007)2025

MAUDE reports naming product code JTZ, 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—11
20090—20
20100—00
20110—11
20120—00
20130—00
20141—00
20150—00
20160—00
20170—10
20180—00
20190—00
20200—00
20210—020
20220—027
20230—020
20240—09
20250—120
20261—0—
FIG. 1 — JTZ by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in JTZ? 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 866.1700.