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S21 OTC Transcutaneous Electrical Nerve Stimulator

K233095 Class II Traditional
Decision Date
2024-03-01
Sponsor / Applicant
Micro Current Technology, Inc.

Technical Specification

510(k) Submission ID K233095
Product Code NUH
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.5890
Decision Date 2024-03-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

S21 OTC Transcutaneous Electrical Nerve Stimulator received FDA 510(k) clearance under submission number K233095, sponsored by Micro Current Technology, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2024-03-01.

Classification & Regulation

This clearance is catalogued under FDA product code NUH and 21 CFR 882.5890, within the Neurology review panel as a Class II device.