FDA 510(k)

ARC可调节桡动脉袖带压缩装置

K号: K173563 · 2018-01-10

决定日期2018-01-10

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

ARC ADJUSTABLE RADIAL CUFF COMPRESSION DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Tz Medical, Inc.. It received FDA 510(k) clearance on 2018-01-10 under 510(k) number K173563. 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 ARC ADJUSTABLE RADIAL CUFF COMPRESSION DEVICE?

ARC ADJUSTABLE RADIAL CUFF COMPRESSION DEVICE is a medical device that received FDA 510(k) clearance on 2018-01-10. The listed applicant is Tz Medical, Inc.. The 510(k) number is K173563.

When did ARC ADJUSTABLE RADIAL CUFF COMPRESSION DEVICE receive FDA 510(k) clearance?

ARC ADJUSTABLE RADIAL CUFF COMPRESSION DEVICE received FDA 510(k) clearance on 2018-01-10, under 510(k) number K173563.

Who is the listed applicant for ARC ADJUSTABLE RADIAL CUFF COMPRESSION DEVICE?

The FDA 510(k) record lists Tz Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ARC ADJUSTABLE RADIAL CUFF COMPRESSION DEVICE?

The FDA product code for ARC ADJUSTABLE RADIAL CUFF COMPRESSION DEVICE is DXC.

列明Tz Medical, Inc.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。

K252772Arc Adjustable Radial Cuff Compression Device K163322TZ颅骨钉成人

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。