510(k) Report

FDA applicant

Applied Technology Ventures, LLC

Rockville, MD2 decisions1997–19980 recalls

FDA records 2 decisions for Applied Technology Ventures, LLC (Rockville, MD) from 1997 to 1998: 2 510(k) clearances. Most are in product codes LDJ (Enzyme Immunoassay, Cannabinoids) and DKZ (Enzyme Immunoassay, Amphetamine). 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 Applied Technology Ventures, LLC’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Applied Technology Ventures, LLC since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Applied Technology Ventures, LLC by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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

See the 510(k) Report

Which product codes does it file in?

  • LDJEnzyme Immunoassay, Cannabinoids1decision
  • DKZEnzyme Immunoassay, Amphetamine1decision

What has FDA decided for it lately?

  • K980836Genie Cup Integrated Screening DeviceApplied Technology Ventures, LLC · 1998
  • K973726Fingerprint Drug Screening DeviceApplied Technology Ventures, LLC · 1997

All 2 as Applied Technology Ventures, LLC →