510(k) Report

FDA applicant

Nu Age Products

Palmdale, CA1 decision1992–19920 recalls

FDA records 1 decision for Nu Age Products (Palmdale, CA) in 1992: 1 510(k) clearance. All are in product code IYZ (Bed, Scanning, 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 Nu Age Products’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Nu Age Products since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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