510(k) Report

FDA applicant

Global Business, Inc.

Midlothian, VA1 decision1990–19900 recalls

FDA records 1 decision for Global Business, Inc. (Midlothian, VA) in 1990: 1 510(k) clearance. All are in product code BYW (Device, Rebreathing). 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 Global Business, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Global Business, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Global Business, 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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