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Talent-Pro Electromagnetic Stimulator

K202031 Class II Traditional
Decision Date
2021-05-06
Sponsor / Applicant
Remed Co., Ltd.

Technical Specification

510(k) Submission ID K202031
Product Code IPF
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5850
Decision Date 2021-05-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Talent-Pro Electromagnetic Stimulator received FDA 510(k) clearance under submission number K202031, sponsored by Remed Co., Ltd.. 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 2021-05-06.

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.