FDA 510(k)

REFINITY旋转IVUS导管，REFINITY旋转IVUS导管，短尖端

K号: K160583 · 2016-10-26

决定日期2016-10-26

产品代码OBJ

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

REFINITY Rotational IVUS Catheter, REFINITY Rotational IVUS Catheter, Short Tip is the device name listed in this FDA 510(k) record. The listed applicant is Volcano Corporation. It received FDA 510(k) clearance on 2016-10-26 under 510(k) number K160583. The device is classified under product code OBJ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the REFINITY Rotational IVUS Catheter, REFINITY Rotational IVUS Catheter, Short Tip?

REFINITY Rotational IVUS Catheter, REFINITY Rotational IVUS Catheter, Short Tip is a medical device that received FDA 510(k) clearance on 2016-10-26. The listed applicant is Volcano Corporation. The 510(k) number is K160583.

When did REFINITY Rotational IVUS Catheter, REFINITY Rotational IVUS Catheter, Short Tip receive FDA 510(k) clearance?

REFINITY Rotational IVUS Catheter, REFINITY Rotational IVUS Catheter, Short Tip received FDA 510(k) clearance on 2016-10-26, under 510(k) number K160583.

Who is the listed applicant for REFINITY Rotational IVUS Catheter, REFINITY Rotational IVUS Catheter, Short Tip?

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

What is the FDA product code for REFINITY Rotational IVUS Catheter, REFINITY Rotational IVUS Catheter, Short Tip?

The FDA product code for REFINITY Rotational IVUS Catheter, REFINITY Rotational IVUS Catheter, Short Tip is OBJ.

列明Volcano 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。

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相关器械（代码：OBJ）

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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