FDA 510(k)

捕手交换设备

K号: K162253 · 2017-01-06

申请人Creganna Medical Aslo Business AS Cregganna Tactx Medical

决定日期2017-01-06

产品代码DQY

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

Trapper Exchange Device is the device name listed in this FDA 510(k) record. The listed applicant is Creganna Medical Aslo Business AS Cregganna Tactx Medical. It received FDA 510(k) clearance on 2017-01-06 under 510(k) number K162253. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Trapper Exchange Device?

Trapper Exchange Device is a medical device that received FDA 510(k) clearance on 2017-01-06. The listed applicant is Creganna Medical Aslo Business AS Cregganna Tactx Medical. The 510(k) number is K162253.

When did Trapper Exchange Device receive FDA 510(k) clearance?

Trapper Exchange Device received FDA 510(k) clearance on 2017-01-06, under 510(k) number K162253.

Who is the listed applicant for Trapper Exchange Device?

The FDA 510(k) record lists Creganna Medical Aslo Business AS Cregganna Tactx Medical as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Trapper Exchange Device?

The FDA product code for Trapper Exchange Device is DQY.

列明Creganna Medical Aslo Business AS Cregganna Tactx Medical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。

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