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FDA 510(k)

Well-life 商标笔式注射针,Well-life 商标安全笔式注射针

K号: K210748 · 2022-05-25

决定日期2022-05-25
产品代码FMI
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

Well-life TM Pen Needles, Well-life TM Safety Pen Needles is the device name listed in this FDA 510(k) record. The listed applicant is W. L. Med Co., Ltd.. It received FDA 510(k) clearance on 2022-05-25 under 510(k) number K210748. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Well-life TM Pen Needles, Well-life TM Safety Pen Needles?

Well-life TM Pen Needles, Well-life TM Safety Pen Needles is a medical device that received FDA 510(k) clearance on 2022-05-25. The listed applicant is W. L. Med Co., Ltd.. The 510(k) number is K210748.

When did Well-life TM Pen Needles, Well-life TM Safety Pen Needles receive FDA 510(k) clearance?

Well-life TM Pen Needles, Well-life TM Safety Pen Needles received FDA 510(k) clearance on 2022-05-25, under 510(k) number K210748.

Who is the listed applicant for Well-life TM Pen Needles, Well-life TM Safety Pen Needles?

The FDA 510(k) record lists W. L. Med Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Well-life TM Pen Needles, Well-life TM Safety Pen Needles?

The FDA product code for Well-life TM Pen Needles, Well-life TM Safety Pen Needles is FMI.

相关临床试验

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相关器械(代码:FMI)

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。

官方来源

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