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QB1 System Powered Muscle Stimulator & Transcutaneous Electrical Nerve Stimulator

K150413 Class II Traditional
Decision Date
2015-04-02
Sponsor / Applicant
Cymedica Orthopedics, Inc.

Technical Specification

510(k) Submission ID K150413
Product Code IPF
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5850
Decision Date 2015-04-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

QB1 System Powered Muscle Stimulator & Transcutaneous Electrical Nerve Stimulator received FDA 510(k) clearance under submission number K150413, sponsored by Cymedica Orthopedics, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 2015-04-02.

Classification & Regulation

This clearance is catalogued under FDA product code IPF and 21 CFR 890.5850, within the Physical Medicine review panel as a Class II device.