Electronic Muscle Stimulator (Model MP01)
K-Number: K233035 · 2024-01-08
Device Summary
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.