电子肌肉刺激器（型号MP01）
K号: K233035 · 2024-01-08
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决定日期2024-01-08
产品代码NGX
咨询委员会PM
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决定实质等同
器械摘要
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.
常见问题
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.
相关临床试验
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相关器械（代码：NGX）
关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。
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官方来源
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