FDA 510(k)

一觸避孕套含苯佐卡因

K 號：K171213 · 2018-01-12

申請人Thai Nippon Rubber Industry Public Company Limited.

決定日期2018-01-12

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

One Touch Condom with Benzocaine is the device name listed in this FDA 510(k) record. The listed applicant is Thai Nippon Rubber Industry Public Company Limited.. It received FDA 510(k) clearance on 2018-01-12 under 510(k) number K171213. 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 One Touch Condom with Benzocaine?

One Touch Condom with Benzocaine is a medical device that received FDA 510(k) clearance on 2018-01-12. The listed applicant is Thai Nippon Rubber Industry Public Company Limited.. The 510(k) number is K171213.

When did One Touch Condom with Benzocaine receive FDA 510(k) clearance?

One Touch Condom with Benzocaine received FDA 510(k) clearance on 2018-01-12, under 510(k) number K171213.

Who is the listed applicant for One Touch Condom with Benzocaine?

The FDA 510(k) record lists Thai Nippon Rubber Industry Public Company Limited. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for One Touch Condom with Benzocaine?

The FDA product code for One Touch Condom with Benzocaine is HIS.

其他以 Thai Nippon Rubber Industry Public Company Limited. 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。

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