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FDA 510(k)

Electronic Muscle Stimulator (Model MP01)

K-Number: K233035 · 2024-01-08

ApplicantShenzhen Hengbosi Industrial Co., Ltd.
Decision Date2024-01-08
Product CodeNGX
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Electronic Muscle Stimulator (Model MP01) is a medical device manufactured by Shenzhen Hengbosi Industrial Co., Ltd.. It received FDA 510(k) clearance on 2024-01-08 under approval number K233035. 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 Electronic Muscle Stimulator (Model MP01)?

Electronic Muscle Stimulator (Model MP01) is a medical device that received FDA 510(k) clearance on 2024-01-08. It is manufactured by Shenzhen Hengbosi Industrial Co., Ltd.. The 510(k) number is K233035.

When was Electronic Muscle Stimulator (Model MP01) approved by the FDA?

Electronic Muscle Stimulator (Model MP01) received FDA 510(k) clearance on 2024-01-08, under approval number K233035.

What company makes Electronic Muscle Stimulator (Model MP01)?

Electronic Muscle Stimulator (Model MP01) is manufactured by Shenzhen Hengbosi Industrial Co., Ltd..

What is the FDA product code for Electronic Muscle Stimulator (Model MP01)?

The FDA product code for Electronic Muscle Stimulator (Model MP01) is NGX.

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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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