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External upper limb tremor stimulator

K182706 Class II Special
Decision Date
2018-10-25
Sponsor / Applicant
Cala Health, Inc.

Technical Specification

510(k) Submission ID K182706
Product Code QBC
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.5897
Decision Date 2018-10-25
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

External upper limb tremor stimulator received FDA 510(k) clearance under submission number K182706, sponsored by Cala Health, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2018-10-25.

Classification & Regulation

This clearance is catalogued under FDA product code QBC and 21 CFR 882.5897, within the Neurology review panel as a Class II device.