510(k) Report

FDA applicant

Alatex Scientific, Inc.

Mountian View, CA1 decision2000–20000 recalls

FDA records 1 decision for Alatex Scientific, Inc. (Mountian View, CA) in 2000: 1 510(k) clearance. All are in product code LDJ (Enzyme Immunoassay, Cannabinoids). 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, clinical toxicology panel, where it files most

How often FDA has decided Alatex Scientific, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Alatex Scientific, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Alatex Scientific, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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