510(k) Report

FDA applicant

Marketing Development Intl.

Mchenry, IL1 decision1976–19760 recalls

FDA records 1 decision for Marketing Development Intl. (Mchenry, IL) in 1976: 1 510(k) clearance. All are in product code JOM (Plethysmograph, Photoelectric, Pneumatic Or…). 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 Marketing Development Intl.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Marketing Development Intl. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Marketing Development Intl. 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.