FDA applicant

Amr Co.

Mchenry, IL1 decision1979–19790 recalls

FDA records 1 decision for Amr Co. (Mchenry, IL) in 1979: 1 510(k) clearance. All are in product code IYY (Synchronizer, Electrocardiograph, Nuclear). 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, radiology panel, where it files most

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

FDA decisions per year

No FDA decision for Amr Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Amr Co.

Which product codes does it file in?

What has FDA decided for it lately?