Bambino 3、S3及S3 Swing、U3及U3 Light、X
K 號：K220698 · 2023-02-16
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器材摘要
Bambino 3, S3 and S3 Swing, U3 and U3 Light, X is the device name listed in this FDA 510(k) record. The listed applicant is Panthera AB. It received FDA 510(k) clearance on 2023-02-16 under 510(k) number K220698. The device is classified under product code IOR. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Bambino 3, S3 and S3 Swing, U3 and U3 Light, X?
Bambino 3, S3 and S3 Swing, U3 and U3 Light, X is a medical device that received FDA 510(k) clearance on 2023-02-16. The listed applicant is Panthera AB. The 510(k) number is K220698.
When did Bambino 3, S3 and S3 Swing, U3 and U3 Light, X receive FDA 510(k) clearance?
Bambino 3, S3 and S3 Swing, U3 and U3 Light, X received FDA 510(k) clearance on 2023-02-16, under 510(k) number K220698.
Who is the listed applicant for Bambino 3, S3 and S3 Swing, U3 and U3 Light, X?
The FDA 510(k) record lists Panthera AB as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Bambino 3, S3 and S3 Swing, U3 and U3 Light, X?
The FDA product code for Bambino 3, S3 and S3 Swing, U3 and U3 Light, X is IOR.
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相關器械（代碼：IOR）
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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