510(k) Report

FDA applicant

Radiology Support Devices, Inc.

Long Beach, CA1 decision1995–19950 recalls

FDA records 1 decision for Radiology Support Devices, Inc. (Long Beach, CA) in 1995: 1 510(k) clearance. All are in product code IYE (Accelerator, Linear, Medical). 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 Radiology Support Devices, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Radiology Support Devices, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Radiology”

FDA records each applicant name separately; these may or may not be the same firm.