FDA 510(k)

可穿戴设备，可穿戴套装

K号: K191272 · 2019-07-12

决定日期2019-07-12

产品代码MSX

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

Wearable Device, Wearable Package is the device name listed in this FDA 510(k) record. The listed applicant is Current Health , Ltd.. It received FDA 510(k) clearance on 2019-07-12 under 510(k) number K191272. The device is classified under product code MSX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Wearable Device, Wearable Package?

Wearable Device, Wearable Package is a medical device that received FDA 510(k) clearance on 2019-07-12. The listed applicant is Current Health , Ltd.. The 510(k) number is K191272.

When did Wearable Device, Wearable Package receive FDA 510(k) clearance?

Wearable Device, Wearable Package received FDA 510(k) clearance on 2019-07-12, under 510(k) number K191272.

Who is the listed applicant for Wearable Device, Wearable Package?

The FDA 510(k) record lists Current Health , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Wearable Device, Wearable Package?

The FDA product code for Wearable Device, Wearable Package is MSX.

列明Current Health , 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。

K231506Current Health System 当前健康系统 K222550Current Health System 当前健康系统 K190073可穿戴设备，带Homehub的便携式收纳盒家庭套餐，不带Homehub的便携式收纳盒家庭套餐

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。