FDA 510(k)

YO家用精子检测

K号: K161493 · 2016-11-08

决定日期2016-11-08

产品代码POV

咨询委员会HE 请注意，由于您只提供了“HE”作为输入，我无法提供完整的翻译。请提供完整的描述或文本，以便我能够进行准确的翻译。

决定实质等同

器械摘要

YO Home Sperm Test is the device name listed in this FDA 510(k) record. The listed applicant is Medical Electronic Systems , Ltd.. It received FDA 510(k) clearance on 2016-11-08 under 510(k) number K161493. The device is classified under product code POV. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the YO Home Sperm Test?

YO Home Sperm Test is a medical device that received FDA 510(k) clearance on 2016-11-08. The listed applicant is Medical Electronic Systems , Ltd.. The 510(k) number is K161493.

When did YO Home Sperm Test receive FDA 510(k) clearance?

YO Home Sperm Test received FDA 510(k) clearance on 2016-11-08, under 510(k) number K161493.

Who is the listed applicant for YO Home Sperm Test?

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

What is the FDA product code for YO Home Sperm Test?

The FDA product code for YO Home Sperm Test is POV.

列明Medical Electronic Systems , 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。

K243114SQA-iOw 精子质量分析仪 K241628YO家用精子检测 K220828SQA-iO 精子质量分析仪

官方来源

在 FDA 数据库中查看 →

数据来源于FDA开放API。如需最新且权威的信息，请务必参考官方记录。