510(k) Report

FDA applicant

Mrt, Inc.

Santa Monica, CA1 decision1991–19910 recalls

FDA records 1 decision for Mrt, Inc. (Santa Monica, CA) in 1991: 1 510(k) clearance. All are in product code ILX (Diathermy, Shortwave, For Use Other Than…). 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, physical medicine panel, where it files most

How often FDA has decided Mrt, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Mrt, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • ILXDiathermy, Shortwave, For Use Other Than Applying Therapeutic Deep Heat1decision

Who builds on its devices?

Later devices cite its devices 3 times; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K903675Magnetic Resonance Therapy DeviceMrt, Inc. · 19913cite it

What has FDA decided for it lately?

  • K903675Magnetic Resonance Therapy DeviceMrt, Inc. · 1991

The one decision as Mrt, Inc. →