510(k) Report

FDA applicant

Global Medical Prods, Inc.

Chicago, IL9 decisions1986–19960 recalls

FDA records 9 decisions for Global Medical Prods, Inc. (Chicago, IL) from 1986 to 1996: 9 510(k) clearances. Most are in product codes FPO (Stretcher, Wheeled) and FCG (Biopsy Needle). 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 Global Medical Prods, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Global Medical Prods, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Global Medical Prods, 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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