FDA applicant

Interad Systems, Inc.

Mchenry, IL4 decisions1981–19840 recalls

FDA records 4 decisions for Interad Systems, Inc. (Mchenry, IL) from 1981 to 1984: 4 510(k) clearances. Most are in product codes IYO (System, Imaging, Pulsed Echo, Ultrasonic) and IYX (Camera, Scintillation (Gamma)). 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, radiology panel, where it files most

How often FDA has decided Interad Systems, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Interad Systems, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Interad Systems, Inc.

Which product codes does it file in?

What has FDA decided for it lately?