510(k) Report

FDA product code · Microbiology

Enzyme Linked Immunosorbent Assay, T. Cruzi

MIUClass I21 CFR 866.3870510(k) required6 decisions since 19921 recall

6 FDA decisions since 1992. 1 recall names this code; it is not Class I. The most-cited predicate is K023889, 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, microbiology panel

Twenty years of MIU 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 · MIU

1in 2016

2009: 12016: 1
2007high 1 (2009) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MIU

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

Recalls per year · MIU

1in 2017

2017: 1
2007high 1 (2017) · low 0 (2007)2026

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

Adverse event reports per year · MIU

3in 2019

2011: 132012: 72013: 72014: 12015: 22016: 52017: 52018: 32019: 3
2007high 13 (2011) · low 0 (2007)2025

MAUDE reports naming product code MIU, 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
20091—00
20100—00
20110—013
20120—07
20130—07
20140—01
20150—02
20161—05
20170—15
20180—03
20190—03
20200—00
20210—00
20220—00
20230—00
20240—00
20250—00
20260—0—
FIG. 1 — MIU by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in MIU? 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 866.3870.