Talent-Pro Electromagnetic Stimulator

FDA 510(k) K202031 · Remed Co., Ltd.

Substantially Equivalent

510(k) numberK202031

Submission

Device name
Talent-Pro Electromagnetic Stimulator
Applicant
Remed Co., Ltd.
Daejeon, KR
Received
July 22, 2020
Decision date
May 6, 2021
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
IPF – Stimulator, Muscle, Powered
Device class
Class II (moderate risk)
Regulation
21 CFR 890.5850
Specialty
Physical Medicine

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Questions and answers

When was Talent-Pro Electromagnetic Stimulator cleared by the FDA?

Talent-Pro Electromagnetic Stimulator (K202031) received a 510(k) decision of Substantially Equivalent on May 6, 2021, 288 days after the submission was received.

What is the product code of K202031?

The FDA product code is IPF – Stimulator, Muscle, Powered, a Class II (moderate risk) device regulated under 21 CFR 890.5850.