Limfa Therapy System (Limfa Therapy)
K号: K243165 · 2025-05-15
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申请人Eywa Srl
决定日期2025-05-15
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
Limfa Therapy System (Limfa Therapy) is the device name listed in this FDA 510(k) record. The listed applicant is Eywa Srl. It received FDA 510(k) clearance on 2025-05-15 under 510(k) number K243165. 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 Limfa Therapy System (Limfa Therapy)?
Limfa Therapy System (Limfa Therapy) is a medical device that received FDA 510(k) clearance on 2025-05-15. The listed applicant is Eywa Srl. The 510(k) number is K243165.
When did Limfa Therapy System (Limfa Therapy) receive FDA 510(k) clearance?
Limfa Therapy System (Limfa Therapy) received FDA 510(k) clearance on 2025-05-15, under 510(k) number K243165.
Who is the listed applicant for Limfa Therapy System (Limfa Therapy)?
The FDA 510(k) record lists Eywa Srl as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Limfa Therapy System (Limfa Therapy)?
The FDA product code for Limfa Therapy System (Limfa Therapy) 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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