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FDA 510(k)

Momcozy可穿戴电动吸奶器(型号:S9 Pro, S12 Pro)

K号: K230776 · 2023-06-09

决定日期2023-06-09
产品代码HGX
咨询委员会OB 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

Momcozy Wearable Electric Breast Pump ( Model: S9 Pro, S12 Pro) is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Lutejiacheng Technology Co., Ltd.. It received FDA 510(k) clearance on 2023-06-09 under 510(k) number K230776. The device is classified under product code HGX. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Momcozy Wearable Electric Breast Pump ( Model: S9 Pro, S12 Pro)?

Momcozy Wearable Electric Breast Pump ( Model: S9 Pro, S12 Pro) is a medical device that received FDA 510(k) clearance on 2023-06-09. The listed applicant is Shenzhen Lutejiacheng Technology Co., Ltd.. The 510(k) number is K230776.

When did Momcozy Wearable Electric Breast Pump ( Model: S9 Pro, S12 Pro) receive FDA 510(k) clearance?

Momcozy Wearable Electric Breast Pump ( Model: S9 Pro, S12 Pro) received FDA 510(k) clearance on 2023-06-09, under 510(k) number K230776.

Who is the listed applicant for Momcozy Wearable Electric Breast Pump ( Model: S9 Pro, S12 Pro)?

The FDA 510(k) record lists Shenzhen Lutejiacheng Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Momcozy Wearable Electric Breast Pump ( Model: S9 Pro, S12 Pro)?

The FDA product code for Momcozy Wearable Electric Breast Pump ( Model: S9 Pro, S12 Pro) is HGX.

相关临床试验

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。

列明Shenzhen Lutejiacheng Technology 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。

相关器械(代码:HGX)

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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