FDA 510(k)

Electromagnetic Stimulator Device(Model EM Contouring and Tesla Duet)

K-Number: K231318 · 2023-07-07

ApplicantBeijing Adss Development Co., Ltd.

Decision Date2023-07-07

Product CodeNGX

Advisory CommitteePM

DecisionSubstantially Equivalent

Device Summary

Electromagnetic Stimulator Device(Model EM Contouring and Tesla Duet) is a medical device manufactured by Beijing Adss Development Co., Ltd.. It received FDA 510(k) clearance on 2023-07-07 under approval number K231318. The device is classified under product code NGX. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Electromagnetic Stimulator Device(Model EM Contouring and Tesla Duet)?

Electromagnetic Stimulator Device(Model EM Contouring and Tesla Duet) is a medical device that received FDA 510(k) clearance on 2023-07-07. It is manufactured by Beijing Adss Development Co., Ltd.. The 510(k) number is K231318.

When was Electromagnetic Stimulator Device(Model EM Contouring and Tesla Duet) approved by the FDA?

Electromagnetic Stimulator Device(Model EM Contouring and Tesla Duet) received FDA 510(k) clearance on 2023-07-07, under approval number K231318.

What company makes Electromagnetic Stimulator Device(Model EM Contouring and Tesla Duet)?

Electromagnetic Stimulator Device(Model EM Contouring and Tesla Duet) is manufactured by Beijing Adss Development Co., Ltd..

What is the FDA product code for Electromagnetic Stimulator Device(Model EM Contouring and Tesla Duet)?

The FDA product code for Electromagnetic Stimulator Device(Model EM Contouring and Tesla Duet) is NGX.

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Related PubMed Literature

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Other Devices by Beijing Adss Development Co., Ltd.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.