FDA 510(k)

Lifetech Cardio 型号 8301 临时起搏器

K号: K182839 · 2019-02-28

申请人Shenzhen Lifetech Cardio Medical Electronics Co., Ltd.

决定日期2019-02-28

产品代码DTE

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

Lifetech Cardio Model 8301 Temporary Pacemaker is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Lifetech Cardio Medical Electronics Co., Ltd.. It received FDA 510(k) clearance on 2019-02-28 under 510(k) number K182839. The device is classified under product code DTE. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Lifetech Cardio Model 8301 Temporary Pacemaker?

Lifetech Cardio Model 8301 Temporary Pacemaker is a medical device that received FDA 510(k) clearance on 2019-02-28. The listed applicant is Shenzhen Lifetech Cardio Medical Electronics Co., Ltd.. The 510(k) number is K182839.

When did Lifetech Cardio Model 8301 Temporary Pacemaker receive FDA 510(k) clearance?

Lifetech Cardio Model 8301 Temporary Pacemaker received FDA 510(k) clearance on 2019-02-28, under 510(k) number K182839.

Who is the listed applicant for Lifetech Cardio Model 8301 Temporary Pacemaker?

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

What is the FDA product code for Lifetech Cardio Model 8301 Temporary Pacemaker?

The FDA product code for Lifetech Cardio Model 8301 Temporary Pacemaker is DTE.

列明Shenzhen Lifetech Cardio Medical Electronics 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。

K232721Lifetech Cardio 临时起搏器

官方来源

在 FDA 数据库中查看 →

数据来源于FDA开放API。如需最新且权威的信息，请务必参考官方记录。