FDA applicant

Multidata Systems International Corp.

St. Louis, MO1 decision1997–19971 recall

FDA records 1 decision for Multidata Systems International Corp. (St. Louis, MO) in 1997: 1 510(k) clearance. All are in product code IYE (Accelerator, Linear, Medical). 1 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, radiology panel, where it files most

How often FDA has decided Multidata Systems International Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Multidata Systems International Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Multidata Systems International Corp.

Which product codes does it file in?

What has FDA decided for it lately?

What has been recalled?