Creme de La Femme 女性潤滑劑
K 號：K180014 · 2018-12-21
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決定日期2018-12-21
產品代碼NUC
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
Creme de La Femme Feminine Lubricant is the device name listed in this FDA 510(k) record. The listed applicant is Cewal, Inc. Dba Premiere Enterprises. It received FDA 510(k) clearance on 2018-12-21 under 510(k) number K180014. The device is classified under product code NUC. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Creme de La Femme Feminine Lubricant?
Creme de La Femme Feminine Lubricant is a medical device that received FDA 510(k) clearance on 2018-12-21. The listed applicant is Cewal, Inc. Dba Premiere Enterprises. The 510(k) number is K180014.
When did Creme de La Femme Feminine Lubricant receive FDA 510(k) clearance?
Creme de La Femme Feminine Lubricant received FDA 510(k) clearance on 2018-12-21, under 510(k) number K180014.
Who is the listed applicant for Creme de La Femme Feminine Lubricant?
The FDA 510(k) record lists Cewal, Inc. Dba Premiere Enterprises as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Creme de La Femme Feminine Lubricant?
The FDA product code for Creme de La Femme Feminine Lubricant is NUC.
相關臨床試驗
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相關器械（代碼：NUC）
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
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。
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