510(k) Report

FDA product code · Microbiology

Test, Immunity, Cell Mediated, Mycobacterium Tuberculosis

NCDClass IIIPMA required2 decisions since 20012 recalls

2 FDA decisions since 2001. 2 recalls name this code, 0 of them Class I.

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 NCD 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 · NCD

10in 2025

2007: 22008: 12010: 32011: 32012: 12014: 42016: 32017: 62018: 52019: 62020: 62021: 62022: 82023: 62024: 62025: 102026 (partial year): 7
2007high 10 (2025) · low 0 (2009)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · NCD

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

Recalls per year · NCD

2in 2012

2012: 2
2007high 2 (2012) · low 0 (2007)2026

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

Adverse event reports per year · NCD

1in 2025

2013: 82015: 62016: 102020: 12024: 22025: 1
2007high 10 (2016) · low 0 (2007)2025

MAUDE reports naming product code NCD, 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
20081—00
20090—00
20103—00
20113—00
20121—20
20130—08
20144—00
20150—06
20163—010
20176—00
20185—00
20196—00
20206—01
20216—00
20228—00
20236—00
20246—02
202510—01
20267—0—
FIG. 1 — NCD by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in NCD? 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