Apapro去敏劑
K 號：K220419 · 2022-02-16
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器材摘要
Apapro Desensitizer is the device name listed in this FDA 510(k) record. The listed applicant is Sangi Co., Ltd.. It received FDA 510(k) clearance on 2022-02-16 under 510(k) number K220419. The device is classified under product code LBH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Apapro Desensitizer?
Apapro Desensitizer is a medical device that received FDA 510(k) clearance on 2022-02-16. The listed applicant is Sangi Co., Ltd.. The 510(k) number is K220419.
When did Apapro Desensitizer receive FDA 510(k) clearance?
Apapro Desensitizer received FDA 510(k) clearance on 2022-02-16, under 510(k) number K220419.
Who is the listed applicant for Apapro Desensitizer?
The FDA 510(k) record lists Sangi Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Apapro Desensitizer?
The FDA product code for Apapro Desensitizer is LBH.
相關臨床試驗
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其他以 Sangi Co., Ltd. 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：LBH）
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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