510(k) Report

FDA applicant

Wilson Medical Instruments Co.

Mchenry, IL1 decision1978–19780 recalls

FDA records 1 decision for Wilson Medical Instruments Co. (Mchenry, IL) in 1978: 1 510(k) clearance. All are in product code DQX (Wire, Guide, Catheter). 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, cardiovascular panel, where it files most

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

FDA decisions per year

No FDA decision for Wilson Medical Instruments Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Wilson Medical Instruments Co. 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?

  • DQXWire, Guide, Catheter1decision

What has FDA decided for it lately?

  • K781561Angiographic Guide WireWilson Medical Instruments Co. · 1978

The one decision as Wilson Medical Instruments Co. →

Other applicant names beginning “Wilson”

FDA records each applicant name separately; these may or may not be the same firm.

Wilson-Cook Medical, Inc. 127Wilson Greatbatch Technologies, Inc. 9Wilson-Cook Medical Inc./Cook Endoscopy 7Wilson Glove Products Co., Ltd. 2Wilson Biomedical, Inc. 2Wilson Instruments (Shanghai) Company Limited 2Wilson Hunt Intl./, Ltd. 1Wilson Tech (International) Limited 1Wilson Instruments (Sha) Co., Ltd. 1