FDA 510(k)

維斯比醫療男性性健康檢測

K 號：K251501 · 2025-10-01

決定日期2025-10-01

產品代碼QEP

諮詢委員會MI (請提供完整的描述文本，以便進行翻譯。)

決定相當於

器材摘要

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.

常見問題

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.

其他以 Visby Medical, Inc. 為申請人之記錄

相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。

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相關器械（代碼：QEP）

相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。

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官方來源

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