510(k) Report

FDA applicant

Wilson Biomedical, Inc.

Glens Falls, NY2 decisions1988–19900 recalls

FDA records 2 decisions for Wilson Biomedical, Inc. (Glens Falls, NY) from 1988 to 1990: 2 510(k) clearances. Most are in product codes DQO (Catheter, Intravascular, Diagnostic) and DQY (Catheter, Percutaneous). 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 Biomedical, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Wilson Biomedical, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Wilson Biomedical, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Which product codes does it file in?

  • DQOCatheter, Intravascular, Diagnostic1decision
  • DQYCatheter, Percutaneous1decision

What has FDA decided for it lately?

  • K892671Wilson Biomedical Angiographic CatheterWilson Biomedical, Inc. · 1990
  • K881793Wilson Biomedical Coronary Guiding CatheterWilson Biomedical, Inc. · 1988

All 2 as Wilson Biomedical, Inc. →

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 Instruments (Shanghai) Company Limited 2Wilson Hunt Intl./, Ltd. 1Wilson Tech (International) Limited 1Wilson Instruments (Sha) Co., Ltd. 1Wilson Medical Instruments Co. 1