TIA 提示，Cariosity，透照輔助針
K 號：K213482 · 2022-04-29
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器材摘要
TIA Tip, Cariosity, Transillumination Accessory Tip is the device name listed in this FDA 510(k) record. The listed applicant is D4D Technologies, LLC. It received FDA 510(k) clearance on 2022-04-29 under 510(k) number K213482. The device is classified under product code NTK. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the TIA Tip, Cariosity, Transillumination Accessory Tip?
TIA Tip, Cariosity, Transillumination Accessory Tip is a medical device that received FDA 510(k) clearance on 2022-04-29. The listed applicant is D4D Technologies, LLC. The 510(k) number is K213482.
When did TIA Tip, Cariosity, Transillumination Accessory Tip receive FDA 510(k) clearance?
TIA Tip, Cariosity, Transillumination Accessory Tip received FDA 510(k) clearance on 2022-04-29, under 510(k) number K213482.
Who is the listed applicant for TIA Tip, Cariosity, Transillumination Accessory Tip?
The FDA 510(k) record lists D4D Technologies, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TIA Tip, Cariosity, Transillumination Accessory Tip?
The FDA product code for TIA Tip, Cariosity, Transillumination Accessory Tip is NTK.
相關臨床試驗
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相關器械（代碼：NTK）
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。
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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