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FDA 510(k)

Muscle Stimulator

K-Number: K231648 · 2024-03-01

ApplicantShenzhen Yiran Intelligent Co., Ltd.
Decision Date2024-03-01
Product CodeNUH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Muscle Stimulator is a medical device manufactured by Shenzhen Yiran Intelligent Co., Ltd.. It received FDA 510(k) clearance on 2024-03-01 under approval number K231648. The device is classified under product code NUH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Muscle Stimulator?

Muscle Stimulator is a medical device that received FDA 510(k) clearance on 2024-03-01. It is manufactured by Shenzhen Yiran Intelligent Co., Ltd.. The 510(k) number is K231648.

When was Muscle Stimulator approved by the FDA?

Muscle Stimulator received FDA 510(k) clearance on 2024-03-01, under approval number K231648.

What company makes Muscle Stimulator?

Muscle Stimulator is manufactured by Shenzhen Yiran Intelligent Co., Ltd..

What is the FDA product code for Muscle Stimulator?

The FDA product code for Muscle Stimulator is NUH.

Related Clinical Trials

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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.

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