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FDA 510(k)

CrossBay IVF 胚胎移植导管套装

K号: K162064 · 2017-01-05

决定日期2017-01-05
产品代码MQF
咨询委员会OB 请注意,由于您没有提供具体的医疗设备监管文本,我无法进行翻译。请提供具体的文本内容,以便我能够按照您的要求进行翻译。
决定实质等同

器械摘要

CrossBay IVF Embryo Transfer Catheter Set is the device name listed in this FDA 510(k) record. The listed applicant is Crossbay Medical, Inc.. It received FDA 510(k) clearance on 2017-01-05 under 510(k) number K162064. The device is classified under product code MQF. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the CrossBay IVF Embryo Transfer Catheter Set?

CrossBay IVF Embryo Transfer Catheter Set is a medical device that received FDA 510(k) clearance on 2017-01-05. The listed applicant is Crossbay Medical, Inc.. The 510(k) number is K162064.

When did CrossBay IVF Embryo Transfer Catheter Set receive FDA 510(k) clearance?

CrossBay IVF Embryo Transfer Catheter Set received FDA 510(k) clearance on 2017-01-05, under 510(k) number K162064.

Who is the listed applicant for CrossBay IVF Embryo Transfer Catheter Set?

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

What is the FDA product code for CrossBay IVF Embryo Transfer Catheter Set?

The FDA product code for CrossBay IVF Embryo Transfer Catheter Set is MQF.

相关临床试验

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相关器械(代码:MQF)

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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