510(k) Report

FDA applicant

Digital Design, Inc.

Norcross, GA1 decision1991–19910 recalls

FDA records 1 decision for Digital Design, Inc. (Norcross, GA) in 1991: 1 510(k) clearance. All are in product code JWM (System, Tomographic, Nuclear). 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 Digital Design, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Digital Design, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Digital Design, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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