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FDA 510(k)

Bambino 3, S3 和 S3 Swing, U3 和 U3 Light, X

K号: K220698 · 2023-02-16

申请人Panthera AB
决定日期2023-02-16
产品代码IOR
咨询委员会PM 请注意,由于您没有提供具体的医疗设备监管文本,我无法进行翻译。请提供具体的文本内容,以便我能够按照您的要求进行翻译。
决定实质等同

器械摘要

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.

常见问题

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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相关器械(代码:IOR)

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系;请查阅链接的官方来源。

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