FDA applicant

Medical Marketing Group

Decatur, GA11 decisions1979–19910 recalls

FDA records 11 decisions for Medical Marketing Group (Decatur, GA) from 1979 to 1991: 11 510(k) clearances. Most are in product codes KNX (Collector, Urine, (And Accessories) For…) and GAZ (Tubing, Noninvasive). 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 Medical Marketing Group’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medical Marketing Group since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Medical Marketing Group

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?