紅外線熱力（型號：E0221）
K 號：K223893 · 2023-05-16
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器材摘要
Infrared Heat (Model: E0221) is the device name listed in this FDA 510(k) record. The listed applicant is Light Tree Ventures Europe B.V.. It received FDA 510(k) clearance on 2023-05-16 under 510(k) number K223893. The device is classified under product code OHS. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Infrared Heat (Model: E0221)?
Infrared Heat (Model: E0221) is a medical device that received FDA 510(k) clearance on 2023-05-16. The listed applicant is Light Tree Ventures Europe B.V.. The 510(k) number is K223893.
When did Infrared Heat (Model: E0221) receive FDA 510(k) clearance?
Infrared Heat (Model: E0221) received FDA 510(k) clearance on 2023-05-16, under 510(k) number K223893.
Who is the listed applicant for Infrared Heat (Model: E0221)?
The FDA 510(k) record lists Light Tree Ventures Europe B.V. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Infrared Heat (Model: E0221)?
The FDA product code for Infrared Heat (Model: E0221) is OHS.
相關臨床試驗
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。
其他以 Light Tree Ventures Europe B.V. 為申請人之記錄
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。
相關器械（代碼：OHS）
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
在 FDA 資料庫中查看 →資料來源為 FDA Open API。如需最新且權威的資訊，請始終參閱官方記錄。
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