510(k) Report

FDA applicant

Clinical MR Solutions, LLC

Brookfield, WI1 decision2003–20030 recalls

FDA records 1 decision for Clinical MR Solutions, LLC (Brookfield, WI) in 2003: 1 510(k) clearance. All are in product code MOS (Coil, Magnetic Resonance, Specialty). 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 Clinical MR Solutions, LLC’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Clinical MR Solutions, LLC since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Clinical MR Solutions, LLC by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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

See the 510(k) Report