510(k) Report

FDA applicant

Kim Institute For Rehabilitation Medicine, P.C.

Midvale, UT1 decision2001–20010 recalls

FDA records 1 decision for Kim Institute For Rehabilitation Medicine, P.C. (Midvale, UT) in 2001: 1 510(k) clearance. All are in product code GXY (Electrode, Cutaneous). 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, neurology panel, where it files most

How often FDA has decided Kim Institute For Rehabilitation Medicine, P.C.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Kim Institute For Rehabilitation Medicine, P.C. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Kim Institute For Rehabilitation Medicine, P.C. 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?

  • GXYElectrode, Cutaneous1decision

What has FDA decided for it lately?

  • K011691Kimstim Auricular ElectrodeKim Institute For Rehabilitation Medicine, P.C. · 2001

The one decision as Kim Institute For Rehabilitation Medicine, P.C. →