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HBOTC Muscle and Nerve Stimulator

K160255 Class II Traditional
Decision Date
2016-09-15
Sponsor / Applicant
Hb Medical, Inc.

Technical Specification

510(k) Submission ID K160255
Product Code NUH
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.5890
Decision Date 2016-09-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HBOTC Muscle and Nerve Stimulator received FDA 510(k) clearance under submission number K160255, sponsored by Hb Medical, 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 2016-09-15.

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.