FDA applicant

Magnetic Resonance Plus, Inc.

Sacramento, CA1 decision1993–19930 recalls

FDA records 1 decision for Magnetic Resonance Plus, Inc. (Sacramento, CA) in 1993: 1 510(k) clearance. All are in product code LNH (System, Nuclear Magnetic Resonance Imaging). 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 Magnetic Resonance Plus, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Magnetic Resonance Plus, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Magnetic Resonance Plus, 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 “Magnetic”

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

Magnetic Research, Inc. 9 Magnetic Resonance Equipment Corp. 5 Magnetic Moments, LLC 1

Magnetic Resonance Plus, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Magnetic”