FDA applicant

Bruce Mclucas

Washington, DC1 decision1994–19940 recalls

FDA records 1 decision for Bruce Mclucas (Washington, DC) in 1994: 1 510(k) clearance. All are in product code HGI (Electrocautery, Gynecologic (And Accessories)). 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, obstetrics and gynecology panel, where it files most

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

FDA decisions per year

No FDA decision for Bruce Mclucas since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Bruce Mclucas’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

Other applicant names beginning “Bruce”

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

Bruce J. Sand M.D. 1 Bruce W. Martin O.D. and Edward Hensley 1 Bruce A. Berkley 1 Bruce Medical Supply 1 Bruce Franklin, Inc. 1

Bruce Mclucas

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Bruce”