FAQ™ (302)
K 號：K242747 · 2024-12-11
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器材摘要
FAQ™ (302) is the device name listed in this FDA 510(k) record. The listed applicant is Foreo, Inc.. It received FDA 510(k) clearance on 2024-12-11 under 510(k) number K242747. The device is classified under product code OAP. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the FAQ™ (302)?
FAQ™ (302) is a medical device that received FDA 510(k) clearance on 2024-12-11. The listed applicant is Foreo, Inc.. The 510(k) number is K242747.
When did FAQ™ (302) receive FDA 510(k) clearance?
FAQ™ (302) received FDA 510(k) clearance on 2024-12-11, under 510(k) number K242747.
Who is the listed applicant for FAQ™ (302)?
The FDA 510(k) record lists Foreo, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FAQ™ (302)?
The FDA product code for FAQ™ (302) is OAP.
其他以 Foreo, Inc. 為申請人之記錄
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相關器械（代碼：OAP）
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
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