FDA applicant

Vulcan Laboratories, Inc.

Birmingham, AL2 decisions1985–19850 recalls

FDA records 2 decisions for Vulcan Laboratories, Inc. (Birmingham, AL) in 1985: 2 510(k) clearances. Most are in product codes JAY (Support, Breathing Tube) and KLK (Monitor, Oxygen, Cutaneous, For Infant Not…). 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, anesthesiology panel, where it files most

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

FDA decisions per year

No FDA decision for Vulcan Laboratories, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Vulcan Laboratories, Inc.

Which product codes does it file in?

What has FDA decided for it lately?