FDA 510(k)

vPATCH

K 號：K223595 · 2023-05-01

決定日期2023-05-01

產品代碼QRC

諮詢委員會GU

決定相當於

器材摘要

vPATCH is the device name listed in this FDA 510(k) record. The listed applicant is Virility Medical , Ltd.. It received FDA 510(k) clearance on 2023-05-01 under 510(k) number K223595. The device is classified under product code QRC. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the vPATCH?

vPATCH is a medical device that received FDA 510(k) clearance on 2023-05-01. The listed applicant is Virility Medical , Ltd.. The 510(k) number is K223595.

When did vPATCH receive FDA 510(k) clearance?

vPATCH received FDA 510(k) clearance on 2023-05-01, under 510(k) number K223595.

Who is the listed applicant for vPATCH?

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

What is the FDA product code for vPATCH?

The FDA product code for vPATCH is QRC.

其他以 Virility Medical , Ltd. 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。

K252809in2 智能型（in2S）

相關器械（代碼：QRC）

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。

K252809in2 智能型（in2S）Virility Medical , Ltd.K241897MORMorari, Inc.

官方來源

在 FDA 資料庫中查看 →

資料來源為 FDA Open API。如需最新且權威的資訊，請始終參閱官方記錄。