QBC · External Upper Limb Tremor Stimulator

Neurology · 21 CFR 882.5897 · Class 2

Overview

Product CodeQBC
Device NameExternal Upper Limb Tremor Stimulator
Regulation21 CFR 882.5897
Device ClassClass 2
Review PanelNeurology

Identification

An external upper limb tremor stimulator is a prescription device which is placed externally on the upper limb and designed to aid in tremor symptom relief of the upper limb.

Classification Rationale

Class II (special controls). The special controls for this device are:

Special Controls

In combination with the general controls of the FD&C Act, the external upper limb tremor stimulator is subject to the following special controls:

*Classification.* Class II (special controls). The special controls for this device are:(1) Non-clinical performance testing must assess the following: (i) Characterization of the electrical stimulation, including the following, must be performed: Waveforms, output modes, maximum output voltage, maximum output current, pulse duration, frequency, net charge per pulse, maximum phase charge at 500 ohms, maximum current density, maximum average current, and maximum average power density. (ii) Impedance testing, current distribution across the electrode surface area, adhesive integrity, and shelf life testing of the electrodes and gels must be conducted. (iii) Simulated use testing of sensor performance and the associated algorithms that determine the stimulation output must be conducted. (2) Patient-contacting components of the device must be demonstrated to be biocompatible. (3) Performance testing must demonstrate electrical, thermal, and mechanical safety along with electromagnetic compatibility (EMC) of the device in the intended use environment. (4) Software verification, validation, and hazard analysis must be performed. (5) Physician and patient labeling must include: (i) Summaries of electrical stimulation parameters; (ii) Instructions on how to correctly use and maintain the device; (iii) Instructions and explanations of all user-interface components; (iv) Instructions on how to clean the device; (v) A shelf life for the electrodes and gel; and (vi) Reuse information.

Recent Cleared Devices (9 of 9)

RecordDevice NameApplicantDecision DateDecision
K253587Cala kIQ PlusCala Health, Inc.Mar 17, 2026SESE
K251517Encora X1Encora, Inc.Feb 5, 2026SESE
K250096Felix NeuroAI SystemFasikl IncorporatedJul 1, 2025SESE
K243848Cala kIQCala Health, Inc.Jan 16, 2025SESE
K242259Cala kIQCala Health, Inc.Nov 22, 2024SESE
K222237Cala kIQCala Health, Inc.Nov 22, 2022SESE
K203288Cala TrioCala Health, Inc.Oct 5, 2021SESE
K182706External upper limb tremor stimulatorCala Health, Inc.Oct 25, 2018SESE
DEN170028Cala ONECala Health, Inc.Apr 26, 2018DENG

Top Applicants

Innolitics

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