FDA 510(k)

Devon 52序贯压缩设备

K号: K182150 · 2018-12-18

申请人Devon Medical Products (Jiangsu), Ltd.

决定日期2018-12-18

产品代码JOW

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

Devon 52 Sequential Compression Device is the device name listed in this FDA 510(k) record. The listed applicant is Devon Medical Products (Jiangsu), Ltd.. It received FDA 510(k) clearance on 2018-12-18 under 510(k) number K182150. The device is classified under product code JOW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Devon 52 Sequential Compression Device?

Devon 52 Sequential Compression Device is a medical device that received FDA 510(k) clearance on 2018-12-18. The listed applicant is Devon Medical Products (Jiangsu), Ltd.. The 510(k) number is K182150.

When did Devon 52 Sequential Compression Device receive FDA 510(k) clearance?

Devon 52 Sequential Compression Device received FDA 510(k) clearance on 2018-12-18, under 510(k) number K182150.

Who is the listed applicant for Devon 52 Sequential Compression Device?

The FDA 510(k) record lists Devon Medical Products (Jiangsu), Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Devon 52 Sequential Compression Device?

The FDA product code for Devon 52 Sequential Compression Device is JOW.

列明Devon Medical Products (Jiangsu), 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。

K190423Devon 24D深静脉血栓（DVT）预防治疗系统 K182578Devon 62深静脉血栓（DVT）预防治疗设备 K173528Devon 24R深静脉血栓（DVT）预防治疗系统 K172030Devon 51 K170814Devon 24

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