Lap-Band 系統校準管
K 號：K220455 · 2022-06-07
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器材摘要
Lap-Band System Calibration Tube is the device name listed in this FDA 510(k) record. The listed applicant is Reshape Lifesciences. It received FDA 510(k) clearance on 2022-06-07 under 510(k) number K220455. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Lap-Band System Calibration Tube?
Lap-Band System Calibration Tube is a medical device that received FDA 510(k) clearance on 2022-06-07. The listed applicant is Reshape Lifesciences. The 510(k) number is K220455.
When did Lap-Band System Calibration Tube receive FDA 510(k) clearance?
Lap-Band System Calibration Tube received FDA 510(k) clearance on 2022-06-07, under 510(k) number K220455.
Who is the listed applicant for Lap-Band System Calibration Tube?
The FDA 510(k) record lists Reshape Lifesciences as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Lap-Band System Calibration Tube?
The FDA product code for Lap-Band System Calibration Tube is KNT.
相關臨床試驗
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其他以 Reshape Lifesciences 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：KNT）
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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