FDA 510(k)

SwimCount 精子质量测试

K号: K183602 · 2019-06-27

决定日期2019-06-27

产品代码POV

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决定实质等同

器械摘要

SwimCount Sperm Quality Test is the device name listed in this FDA 510(k) record. The listed applicant is Motilitycount Aps. It received FDA 510(k) clearance on 2019-06-27 under 510(k) number K183602. 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 SwimCount Sperm Quality Test?

SwimCount Sperm Quality Test is a medical device that received FDA 510(k) clearance on 2019-06-27. The listed applicant is Motilitycount Aps. The 510(k) number is K183602.

When did SwimCount Sperm Quality Test receive FDA 510(k) clearance?

SwimCount Sperm Quality Test received FDA 510(k) clearance on 2019-06-27, under 510(k) number K183602.

Who is the listed applicant for SwimCount Sperm Quality Test?

The FDA 510(k) record lists Motilitycount Aps as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SwimCount Sperm Quality Test?

The FDA product code for SwimCount Sperm Quality Test is POV.

列明Motilitycount Aps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。

K241348SwimCount® 收割器（1 mL）；SwimCount® 收割器（3 mL）

官方来源

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