林法療法系統（林法療法）
K 號：K243165 · 2025-05-15
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器材摘要
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.
常見問題
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.
相關臨床試驗
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相關器械（代碼：NGX）
相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。
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官方來源
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