清朗
K 號：K242438 · 2025-05-16
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器材摘要
Clearo is the device name listed in this FDA 510(k) record. The listed applicant is Breas Medical AB. It received FDA 510(k) clearance on 2025-05-16 under 510(k) number K242438. The device is classified under product code NHJ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Clearo?
Clearo is a medical device that received FDA 510(k) clearance on 2025-05-16. The listed applicant is Breas Medical AB. The 510(k) number is K242438.
When did Clearo receive FDA 510(k) clearance?
Clearo received FDA 510(k) clearance on 2025-05-16, under 510(k) number K242438.
Who is the listed applicant for Clearo?
The FDA 510(k) record lists Breas Medical AB as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Clearo?
The FDA product code for Clearo is NHJ.
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其他以 Breas Medical AB 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：NHJ）
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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