FDA 510(k)

MIVI Q 远端通路导管

K号: K212402 · 2021-12-16

决定日期2021-12-16

产品代码QJP

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

MIVI Q Distal Access Catheter is the device name listed in this FDA 510(k) record. The listed applicant is Mivi Neuroscience, Inc.. It received FDA 510(k) clearance on 2021-12-16 under 510(k) number K212402. The device is classified under product code QJP. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the MIVI Q Distal Access Catheter?

MIVI Q Distal Access Catheter is a medical device that received FDA 510(k) clearance on 2021-12-16. The listed applicant is Mivi Neuroscience, Inc.. The 510(k) number is K212402.

When did MIVI Q Distal Access Catheter receive FDA 510(k) clearance?

MIVI Q Distal Access Catheter received FDA 510(k) clearance on 2021-12-16, under 510(k) number K212402.

Who is the listed applicant for MIVI Q Distal Access Catheter?

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

What is the FDA product code for MIVI Q Distal Access Catheter?

The FDA product code for MIVI Q Distal Access Catheter is QJP.

列明Mivi Neuroscience, 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。

K222948Q 远端通路导管 K163233MIVI 6F 25cm Mi-EXT 扩展导管，MIVI 5F 25cm Mi-EXT 扩展导管，MIVI 4F 30cm Mi-EXT 扩展导管，MIVI 3F 43cm Mi-EXT 扩展导管

官方来源

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