510(k) Report

FDA applicant

Euro-American Marketing Group, Inc.

Mount Prospect, IL3 decisions1988–19900 recalls

FDA records 3 decisions for Euro-American Marketing Group, Inc. (Mount Prospect, IL) from 1988 to 1990: 3 510(k) clearances. Most are in product codes JJQ (Colorimeter, Photometer, Spectrophotometer For…) and DXH (Transmitters And Receivers…). 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, clinical chemistry panel, where it files most

How often FDA has decided Euro-American Marketing Group, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Euro-American Marketing Group, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Euro-American Marketing Group, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • JJQColorimeter, Photometer, Spectrophotometer For Clinical Use1decision
  • DXHTransmitters And Receivers, Electrocardiograph, Telephone1decision
  • GADRetractor1decision

What has FDA decided for it lately?

  • K903164Euramark 610 PhotometerEuro-American Marketing Group, Inc. · 1990
  • K894856CardiophoneEuro-American Marketing Group, Inc. · 1990
  • K882112Murse RetractorEuro-American Marketing Group, Inc. · 1988

All 3 as Euro-American Marketing Group, Inc. →