FDA applicant

Thomas J. Fogarty, M.D.

Mchenry, IL6 decisions1983–19900 recalls

FDA records 6 decisions for Thomas J. Fogarty, M.D. (Mchenry, IL) from 1983 to 1990: 6 510(k) clearances. Most are in product codes KNQ (Dilator, Esophageal) and DRS (Transducer, Blood-Pressure, Extravascular). 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, gastroenterology and urology panel, where it files most

How often FDA has decided Thomas J. Fogarty, M.D.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Thomas J. Fogarty, M.D. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Thomas J. Fogarty, M.D. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Thomas J. Fogarty, M.D.’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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Other applicant names beginning “Thomas”

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

Thomas Medical Products, Inc. 23 Thomas Industries 9 Thomas Medical, Inc. 2 Thomas M. Foti, M.D. 1 Thomas G. Mason 1 Thomas Surgical Instruments, Inc. 1

Thomas J. Fogarty, M.D.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Thomas”