FDA applicant

Syncor Radiation Management

Cleveland, OH1 decision2003–20030 recalls

FDA records 1 decision for Syncor Radiation Management (Cleveland, OH) in 2003: 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 Syncor Radiation Management’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Syncor Radiation Management since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Syncor”

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

Syncor Intl. Corp. 31 Syncor Pharmaceuticals, Inc. 4 Syncor International, Inc. 2

Syncor Radiation Management

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Syncor”