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FDA 510(k)

Electronic Muscle Stimulator (Model MP01)

K-Number: K233035 · 2024-01-08

Decision Date2024-01-08
Product CodeNGX
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Electronic Muscle Stimulator (Model MP01) is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Hengbosi Industrial Co., Ltd.. It received FDA 510(k) clearance on 2024-01-08 under 510(k) 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. The listed applicant is Shenzhen Hengbosi Industrial Co., Ltd.. The 510(k) number is K233035.

When did Electronic Muscle Stimulator (Model MP01) receive FDA 510(k) clearance?

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

Who is the listed applicant for Electronic Muscle Stimulator (Model MP01)?

The FDA 510(k) record lists Shenzhen Hengbosi Industrial Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

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

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

Related Devices (Code: NGX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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