FDA applicant

Burney Products Corp.

Brooklyn, NY1 decision1988–19880 recalls

FDA records 1 decision for Burney Products Corp. (Brooklyn, NY) in 1988: 1 510(k) clearance. All are in product code LDQ (Unnamed device). 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, general hospital panel, where it files most

How often FDA has decided Burney Products Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Burney Products Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Burney Products Corp.

Which product codes does it file in?

What has FDA decided for it lately?