FDA 510(k)

LensHooke X1 PRO 精子质量分析仪，LensHooke X1 PRO SE 精子质量分析仪

K号: K202089 · 2020-10-28

决定日期2020-10-28

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

LensHooke X1 PRO Semen Quality Analyzer, LensHooke X1 PRO SE Semen Quality Analyzer is the device name listed in this FDA 510(k) record. The listed applicant is Bonraybio Co., Ltd.. It received FDA 510(k) clearance on 2020-10-28 under 510(k) number K202089. 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 LensHooke X1 PRO Semen Quality Analyzer, LensHooke X1 PRO SE Semen Quality Analyzer?

LensHooke X1 PRO Semen Quality Analyzer, LensHooke X1 PRO SE Semen Quality Analyzer is a medical device that received FDA 510(k) clearance on 2020-10-28. The listed applicant is Bonraybio Co., Ltd.. The 510(k) number is K202089.

When did LensHooke X1 PRO Semen Quality Analyzer, LensHooke X1 PRO SE Semen Quality Analyzer receive FDA 510(k) clearance?

LensHooke X1 PRO Semen Quality Analyzer, LensHooke X1 PRO SE Semen Quality Analyzer received FDA 510(k) clearance on 2020-10-28, under 510(k) number K202089.

Who is the listed applicant for LensHooke X1 PRO Semen Quality Analyzer, LensHooke X1 PRO SE Semen Quality Analyzer?

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

What is the FDA product code for LensHooke X1 PRO Semen Quality Analyzer, LensHooke X1 PRO SE Semen Quality Analyzer?

The FDA product code for LensHooke X1 PRO Semen Quality Analyzer, LensHooke X1 PRO SE Semen Quality Analyzer is POV.

列明Bonraybio 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。

K242830LensHooke X3 PRO 精子质量分析仪；LensHooke X3 PRO SE 精子质量分析仪 K242388LensHooke X12 PRO 精子分析系统 K221810LensHooke CA1 精子分离装置，LensHooke CA0 精子分离装置 K180343LensHooke X1 Pro 精子质量分析仪，LensHooke X1 精子质量分析仪

官方来源

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