FDA 510(k)

Glidewire GT

K号: K170417 · 2017-09-15

决定日期2017-09-15

产品代码DQX

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

Glidewire GT is the device name listed in this FDA 510(k) record. The listed applicant is Terumo Corporation. It received FDA 510(k) clearance on 2017-09-15 under 510(k) number K170417. The device is classified under product code DQX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Glidewire GT?

Glidewire GT is a medical device that received FDA 510(k) clearance on 2017-09-15. The listed applicant is Terumo Corporation. The 510(k) number is K170417.

When did Glidewire GT receive FDA 510(k) clearance?

Glidewire GT received FDA 510(k) clearance on 2017-09-15, under 510(k) number K170417.

Who is the listed applicant for Glidewire GT?

The FDA 510(k) record lists Terumo Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Glidewire GT?

The FDA product code for Glidewire GT is DQX.

列明Terumo Corporation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。

K252295Ryurei K250700笔式注射器针头 32.5 K250751DualView导管 K240818R2P Radifocus Glidewire Advantage K240859Glidewire GT-R K190427Immucise

查看所有 9 个设备 →

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。