FDA 510(k)

Gems 卵母細胞回收緩冲液 ORB-20，ORB-50

K 號：K170498 · 2017-09-28

決定日期2017-09-28

產品代碼MQL

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

Gems Oocyte Retrieval Buffer ORB-20, ORB-50 is the device name listed in this FDA 510(k) record. The listed applicant is Genea Biomedx Pty, Ltd.. It received FDA 510(k) clearance on 2017-09-28 under 510(k) number K170498. The device is classified under product code MQL. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Gems Oocyte Retrieval Buffer ORB-20, ORB-50?

Gems Oocyte Retrieval Buffer ORB-20, ORB-50 is a medical device that received FDA 510(k) clearance on 2017-09-28. The listed applicant is Genea Biomedx Pty, Ltd.. The 510(k) number is K170498.

When did Gems Oocyte Retrieval Buffer ORB-20, ORB-50 receive FDA 510(k) clearance?

Gems Oocyte Retrieval Buffer ORB-20, ORB-50 received FDA 510(k) clearance on 2017-09-28, under 510(k) number K170498.

Who is the listed applicant for Gems Oocyte Retrieval Buffer ORB-20, ORB-50?

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

What is the FDA product code for Gems Oocyte Retrieval Buffer ORB-20, ORB-50?

The FDA product code for Gems Oocyte Retrieval Buffer ORB-20, ORB-50 is MQL.

其他以 Genea Biomedx Pty, Ltd. 為申請人之記錄

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相關器械（代碼：MQL）

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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