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FDA 510(k)

MagXtract 收集管

K 號：K212113 · 2022-07-28

申請人Magbio Genomics, Inc.
決定日期2022-07-28
產品代碼QBD
諮詢委員會MI (請提供完整的描述文本，以便進行翻譯。)
決定相當於

器材摘要

MagXtract Collection Tube is the device name listed in this FDA 510(k) record. The listed applicant is Magbio Genomics, Inc.. It received FDA 510(k) clearance on 2022-07-28 under 510(k) number K212113. The device is classified under product code QBD. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the MagXtract Collection Tube?

MagXtract Collection Tube is a medical device that received FDA 510(k) clearance on 2022-07-28. The listed applicant is Magbio Genomics, Inc.. The 510(k) number is K212113.

When did MagXtract Collection Tube receive FDA 510(k) clearance?

MagXtract Collection Tube received FDA 510(k) clearance on 2022-07-28, under 510(k) number K212113.

Who is the listed applicant for MagXtract Collection Tube?

The FDA 510(k) record lists Magbio Genomics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MagXtract Collection Tube?

The FDA product code for MagXtract Collection Tube is QBD.

相關臨床試驗

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。

NCT07608549FLASH 預試階段 1 安全性研究NOT_YET_RECRUITINGNCT06562205PAP系統外部臨床研究（ECS）NOT_YET_RECRUITINGNCT06443177對於動脈瘤性硬腦膜下出血引起的腦血管收縮，交感調節的影響SUSPENDEDNCT07095751人工智能協助的Uro-Cam導尿管評估系統，用於診斷膀胱癌NOT_YET_RECRUITING

相關器械（代碼：QBD）

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。

K242820普里坦 PurSafe Plus 收集及運輸系統Puritan Medical Products, LLCK240797PPH 唾液收集套件Permantis Public HealthK222771樣本防腐劑液Hangzhou Bioer Technology Co., Ltd.K233324分子傳遞媒體 - MTMAlb LuzK221547InActiv藍Fertipro NVK212878樣本保存解決方案Zhejiang Gene Science Co., Ltd.

官方來源

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