BEAR 及 BEAR mini
K 號：K200803 · 2020-07-31
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器材摘要
BEAR and BEAR mini is the device name listed in this FDA 510(k) record. The listed applicant is Foreo, Inc.. It received FDA 510(k) clearance on 2020-07-31 under 510(k) number K200803. The device is classified under product code NFO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the BEAR and BEAR mini?
BEAR and BEAR mini is a medical device that received FDA 510(k) clearance on 2020-07-31. The listed applicant is Foreo, Inc.. The 510(k) number is K200803.
When did BEAR and BEAR mini receive FDA 510(k) clearance?
BEAR and BEAR mini received FDA 510(k) clearance on 2020-07-31, under 510(k) number K200803.
Who is the listed applicant for BEAR and BEAR mini?
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 BEAR and BEAR mini?
The FDA product code for BEAR and BEAR mini is NFO.
其他以 Foreo, Inc. 為申請人之記錄
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相關器械（代碼：NFO）
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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