FDA 510(k)

Sunmed一次性血管闭合垫

K号: K191827 · 2020-03-16

申请人Sunny Medical Device (Shenzhen) Co., Ltd.

决定日期2020-03-16

产品代码DXC

咨询委员会CV 请注意，由于原文未提供具体内容，以下是一个示例翻译： --- 产品名称：[产品名称] 公司名称：[公司名称] FDA批准号：[FDA批准号] 510(k)申请号：[510(k)申请号] PMA申请号：[PMA申请号] 临床试验注册号：[NCT] PubMed ID：[PMID] 产品标识符：[标识符] 产品URL：[URL] --- 请将上述示例中的[产品名称]、[公司名称]、[FDA批准号]等占位符替换为实际内容。

决定实质等同

器械摘要

Sunmed Disposable Angio-Closure Pads is the device name listed in this FDA 510(k) record. The listed applicant is Sunny Medical Device (Shenzhen) Co., Ltd.. It received FDA 510(k) clearance on 2020-03-16 under 510(k) number K191827. The device is classified under product code DXC. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Sunmed Disposable Angio-Closure Pads?

Sunmed Disposable Angio-Closure Pads is a medical device that received FDA 510(k) clearance on 2020-03-16. The listed applicant is Sunny Medical Device (Shenzhen) Co., Ltd.. The 510(k) number is K191827.

When did Sunmed Disposable Angio-Closure Pads receive FDA 510(k) clearance?

Sunmed Disposable Angio-Closure Pads received FDA 510(k) clearance on 2020-03-16, under 510(k) number K191827.

Who is the listed applicant for Sunmed Disposable Angio-Closure Pads?

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

What is the FDA product code for Sunmed Disposable Angio-Closure Pads?

The FDA product code for Sunmed Disposable Angio-Closure Pads is DXC.

列明Sunny Medical Device (Shenzhen) 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。

K160190Sunmed控制注射器 K153685Sunmed止血阀

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