510(k) Report

FDA applicant

Drial Consultants, Inc.

Simi Valley, CA13 decisions1997–19980 recalls

FDA records 13 decisions for Drial Consultants, Inc. (Simi Valley, CA) from 1997 to 1998: 13 510(k) clearances. Most are in product codes DKZ (Enzyme Immunoassay, Amphetamine) and JXM (Enzyme Immunoassay, Benzodiazepine). 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 Drial Consultants, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Drial Consultants, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Drial Consultants, 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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