FDA applicant

Intelligence Artificielle Applications

Washington, DC1 decision1999–19990 recalls

FDA records 1 decision for Intelligence Artificielle Applications (Washington, DC) in 1999: 1 510(k) clearance. All are in product code KZK (Reader, Zone, Automated). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, microbiology panel, where it files most

How often FDA has decided Intelligence Artificielle Applications’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Intelligence Artificielle Applications since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Intelligence Artificielle Applications by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Intelligence”

FDA records each applicant name separately; these may or may not be the same firm.

Intelligence IN Medical Technologies 1

Intelligence Artificielle Applications

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Intelligence”