510(k) Report

FDA applicant

Marketing Consultants of America

Walker, MI2 decisions1981–19810 recalls

FDA records 2 decisions for Marketing Consultants of America (Walker, MI) in 1981: 2 510(k) clearances. Most are in product codes FTC (Light, Ultraviolet, Dermatological) and GGG (Guaiac Reagent). 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, general and plastic surgery panel, where it files most

How often FDA has decided Marketing Consultants of America’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Marketing Consultants of America since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Marketing”

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