FDA 510(k)

杜蕾斯帕特倫斯緊密適合，杜蕾斯帕特倫斯標準型

K 號：K220489 · 2022-11-07

決定日期2022-11-07

產品代碼HIS

諮詢委員會OB設備之醫療設備規範文本翻譯如下：關於OB設備的醫療設備規範文件：此設備已通過FDA認證，並獲得510(k)許可證。該設備的PMA申請已提交，並在NCT登錄編號為[編號]的研究中進行測試。相關文獻的PMID編號為[編號]。請參考以下識別碼和網址：識別碼：[識別碼] 網址：[網址] 政策：醫療規範-v1

決定相當於

器材摘要

Durex Patronus CloseFit, Durex Patronus Regular is the device name listed in this FDA 510(k) record. The listed applicant is Rb Health (Us), LLC. It received FDA 510(k) clearance on 2022-11-07 under 510(k) number K220489. The device is classified under product code HIS. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Durex Patronus CloseFit, Durex Patronus Regular?

Durex Patronus CloseFit, Durex Patronus Regular is a medical device that received FDA 510(k) clearance on 2022-11-07. The listed applicant is Rb Health (Us), LLC. The 510(k) number is K220489.

When did Durex Patronus CloseFit, Durex Patronus Regular receive FDA 510(k) clearance?

Durex Patronus CloseFit, Durex Patronus Regular received FDA 510(k) clearance on 2022-11-07, under 510(k) number K220489.

Who is the listed applicant for Durex Patronus CloseFit, Durex Patronus Regular?

The FDA 510(k) record lists Rb Health (Us), LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Durex Patronus CloseFit, Durex Patronus Regular?

The FDA product code for Durex Patronus CloseFit, Durex Patronus Regular is HIS.

其他以 Rb Health (Us), LLC 為申請人之記錄

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相關器械（代碼：HIS）

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。

官方來源

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