FDA applicant

Vq Corp.

Cincinnati, OH1 decision2000–20000 recalls

FDA records 1 decision for Vq Corp. (Cincinnati, OH) in 2000: 1 510(k) clearance. All are in product code DRX (Electrode, Electrocardiograph). 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, cardiovascular panel, where it files most

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

FDA decisions per year

No FDA decision for Vq Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Vq Corp.’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

Vq Corp.

Which product codes does it file in?

What has FDA decided for it lately?