510(k) Report

FDA product code · Microbiology

Kit, Immunochromatographic, Bacillus Anthracis Differential Antibody

NPOClass II21 CFR 866.3045510(k) required1 decision since 20030 recalls

1 FDA decision since 2003. No recall names this code.

A serological reagent to distinguish b. Anthracis culture growth from other bacillus spp. Growth

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 NPO 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 · NPO

FDA has decided no NPO device since 2007.

Median 510(k) review, days · NPO

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

Recalls per year · NPO

No recall names NPO since 2007.

Adverse event reports per year · NPO

1in 2012

2012: 1
2007high 1 (2012) · low 0 (2007)2025

MAUDE reports naming product code NPO, 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
20110—00
20120—01
20130—00
20140—00
20150—00
20160—00
20170—00
20180—00
20190—00
20200—00
20210—00
20220—00
20230—00
20240—00
20250—00
20260—0—
FIG. 1 — NPO by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in NPO? A 510(k) Report ranks candidate predicates in this code by lineage, citations and recall history, with the review-time outlook.

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Related product codes

Other codes under 21 CFR 866.3045.