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FDA 510(k)

DC-30/DC-32/DC-28/DC-26/DC-25 诊断超声系统

K号: K173369 · 2017-12-13

决定日期2017-12-13
产品代码IYN
咨询委员会RA
决定实质等同

器械摘要

DC-30/DC-32/DC-28/DC-26/DC-25 Diagnostic Ultrasound System is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Mindray Bio-Meidcal Electronics Co., Ltd.. It received FDA 510(k) clearance on 2017-12-13 under 510(k) number K173369. The device is classified under product code IYN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the DC-30/DC-32/DC-28/DC-26/DC-25 Diagnostic Ultrasound System?

DC-30/DC-32/DC-28/DC-26/DC-25 Diagnostic Ultrasound System is a medical device that received FDA 510(k) clearance on 2017-12-13. The listed applicant is Shenzhen Mindray Bio-Meidcal Electronics Co., Ltd.. The 510(k) number is K173369.

When did DC-30/DC-32/DC-28/DC-26/DC-25 Diagnostic Ultrasound System receive FDA 510(k) clearance?

DC-30/DC-32/DC-28/DC-26/DC-25 Diagnostic Ultrasound System received FDA 510(k) clearance on 2017-12-13, under 510(k) number K173369.

Who is the listed applicant for DC-30/DC-32/DC-28/DC-26/DC-25 Diagnostic Ultrasound System?

The FDA 510(k) record lists Shenzhen Mindray Bio-Meidcal Electronics Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DC-30/DC-32/DC-28/DC-26/DC-25 Diagnostic Ultrasound System?

The FDA product code for DC-30/DC-32/DC-28/DC-26/DC-25 Diagnostic Ultrasound System is IYN.

相关临床试验

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。

列明Shenzhen Mindray Bio-Meidcal Electronics Co., Ltd.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。

相关器械(代码:IYN)

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。

官方来源

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