FDA 510(k)

维斯比医疗男性性健康检测

K号: K251501 · 2025-10-01

决定日期2025-10-01

产品代码QEP

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决定实质等同

器械摘要

Visby Medical Men's Sexual Health Test is the device name listed in this FDA 510(k) record. The listed applicant is Visby Medical, Inc.. It received FDA 510(k) clearance on 2025-10-01 under 510(k) number K251501. The device is classified under product code QEP. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Visby Medical Men's Sexual Health Test?

Visby Medical Men's Sexual Health Test is a medical device that received FDA 510(k) clearance on 2025-10-01. The listed applicant is Visby Medical, Inc.. The 510(k) number is K251501.

When did Visby Medical Men's Sexual Health Test receive FDA 510(k) clearance?

Visby Medical Men's Sexual Health Test received FDA 510(k) clearance on 2025-10-01, under 510(k) number K251501.

Who is the listed applicant for Visby Medical Men's Sexual Health Test?

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

What is the FDA product code for Visby Medical Men's Sexual Health Test?

The FDA product code for Visby Medical Men's Sexual Health Test is QEP.

列明Visby Medical, Inc.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。

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