快速HB，快速LB，快速MB
K 號：K173318 · 2017-10-31
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器材摘要
Rapid HB, Rapid LB, Rapid MB is the device name listed in this FDA 510(k) record. The listed applicant is 3M Deutschland GmbH. It received FDA 510(k) clearance on 2017-10-31 under 510(k) number K173318. The device is classified under product code ELW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Rapid HB, Rapid LB, Rapid MB?
Rapid HB, Rapid LB, Rapid MB is a medical device that received FDA 510(k) clearance on 2017-10-31. The listed applicant is 3M Deutschland GmbH. The 510(k) number is K173318.
When did Rapid HB, Rapid LB, Rapid MB receive FDA 510(k) clearance?
Rapid HB, Rapid LB, Rapid MB received FDA 510(k) clearance on 2017-10-31, under 510(k) number K173318.
Who is the listed applicant for Rapid HB, Rapid LB, Rapid MB?
The FDA 510(k) record lists 3M Deutschland GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Rapid HB, Rapid LB, Rapid MB?
The FDA product code for Rapid HB, Rapid LB, Rapid MB is ELW.
相關臨床試驗
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其他以 3M Deutschland GmbH 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：ELW）
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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