HI-EMT MAGSHAPE
K号: K230024 · 2023-09-06
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决定日期2023-09-06
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
HI-EMT MAGSHAPE is the device name listed in this FDA 510(k) record. The listed applicant is Beijing Sano Laser S&T Development Co.,Ltd. It received FDA 510(k) clearance on 2023-09-06 under 510(k) number K230024. 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 HI-EMT MAGSHAPE?
HI-EMT MAGSHAPE is a medical device that received FDA 510(k) clearance on 2023-09-06. The listed applicant is Beijing Sano Laser S&T Development Co.,Ltd. The 510(k) number is K230024.
When did HI-EMT MAGSHAPE receive FDA 510(k) clearance?
HI-EMT MAGSHAPE received FDA 510(k) clearance on 2023-09-06, under 510(k) number K230024.
Who is the listed applicant for HI-EMT MAGSHAPE?
The FDA 510(k) record lists Beijing Sano Laser S&T Development Co.,Ltd as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HI-EMT MAGSHAPE?
The FDA product code for HI-EMT MAGSHAPE is NGX.
相关临床试验
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列明Beijing Sano Laser S&T Development Co.,Ltd为申报人的其他记录
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。
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
在 FDA 数据库中查看 →数据来源于FDA开放API。如需最新且权威的信息，请务必参考官方记录。
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