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FDA 510(k)

T-Top 10 & T-Top T-Top 11

K号: K232658 · 2023-11-27

决定日期2023-11-27
产品代码FLE
咨询委员会医疗设备监管文本翻译如下: HO 请注意,由于您没有提供具体的医疗设备监管文本内容,以上仅为示例。请提供具体的文本内容以便进行准确的翻译。
决定实质等同

器械摘要

T-Top 10 & T-Top T-Top 11 is the device name listed in this FDA 510(k) record. The listed applicant is Tuttnauer U.S.A Co, Ltd.. It received FDA 510(k) clearance on 2023-11-27 under 510(k) number K232658. The device is classified under product code FLE. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the T-Top 10 & T-Top T-Top 11?

T-Top 10 & T-Top T-Top 11 is a medical device that received FDA 510(k) clearance on 2023-11-27. The listed applicant is Tuttnauer U.S.A Co, Ltd.. The 510(k) number is K232658.

When did T-Top 10 & T-Top T-Top 11 receive FDA 510(k) clearance?

T-Top 10 & T-Top T-Top 11 received FDA 510(k) clearance on 2023-11-27, under 510(k) number K232658.

Who is the listed applicant for T-Top 10 & T-Top T-Top 11?

The FDA 510(k) record lists Tuttnauer U.S.A Co, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for T-Top 10 & T-Top T-Top 11?

The FDA product code for T-Top 10 & T-Top T-Top 11 is FLE.

相关器械(代码:FLE)

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