Coresculpt & Magsculpt
K号: K222400 · 2024-02-27
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决定日期2024-02-27
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
Coresculpt & Magsculpt is the device name listed in this FDA 510(k) record. The listed applicant is K1Med Co., Ltd.. It received FDA 510(k) clearance on 2024-02-27 under 510(k) number K222400. 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 Coresculpt & Magsculpt?
Coresculpt & Magsculpt is a medical device that received FDA 510(k) clearance on 2024-02-27. The listed applicant is K1Med Co., Ltd.. The 510(k) number is K222400.
When did Coresculpt & Magsculpt receive FDA 510(k) clearance?
Coresculpt & Magsculpt received FDA 510(k) clearance on 2024-02-27, under 510(k) number K222400.
Who is the listed applicant for Coresculpt & Magsculpt?
The FDA 510(k) record lists K1Med Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Coresculpt & Magsculpt?
The FDA product code for Coresculpt & Magsculpt is NGX.
相关临床试验
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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