FDA 510(k)

THERMOCLICK

K号: K222057 · 2023-12-05

决定日期2023-12-05

产品代码FLL

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

THERMOCLICK is the device name listed in this FDA 510(k) record. The listed applicant is T&R BIOFAB CO., Ltd.. It received FDA 510(k) clearance on 2023-12-05 under 510(k) number K222057. The device is classified under product code FLL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the THERMOCLICK?

THERMOCLICK is a medical device that received FDA 510(k) clearance on 2023-12-05. The listed applicant is T&R BIOFAB CO., Ltd.. The 510(k) number is K222057.

When did THERMOCLICK receive FDA 510(k) clearance?

THERMOCLICK received FDA 510(k) clearance on 2023-12-05, under 510(k) number K222057.

Who is the listed applicant for THERMOCLICK?

FDA 510(k)记录将T&R BIOFAB CO., Ltd.列为申请人。这本身并不足以确立该设备制造商的身份。

What is the FDA product code for THERMOCLICK?

The FDA product code for THERMOCLICK is FLL.

列明T&R BIOFAB CO., Ltd.为申报人的其他记录

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。

K251959TnR 颅内植入物

相关器械（代码：FLL）

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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官方来源

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