FDA 510(k)

巴克里基本產後氣球

K 號：K223098 · 2022-10-28

決定日期2022-10-28

產品代碼OQY

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

Bakri Essential Postpartum Balloon is the device name listed in this FDA 510(k) record. The listed applicant is Cook Incorporated. It received FDA 510(k) clearance on 2022-10-28 under 510(k) number K223098. The device is classified under product code OQY. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Bakri Essential Postpartum Balloon?

Bakri Essential Postpartum Balloon is a medical device that received FDA 510(k) clearance on 2022-10-28. The listed applicant is Cook Incorporated. The 510(k) number is K223098.

When did Bakri Essential Postpartum Balloon receive FDA 510(k) clearance?

Bakri Essential Postpartum Balloon received FDA 510(k) clearance on 2022-10-28, under 510(k) number K223098.

Who is the listed applicant for Bakri Essential Postpartum Balloon?

The FDA 510(k) record lists Cook Incorporated as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Bakri Essential Postpartum Balloon?

The FDA product code for Bakri Essential Postpartum Balloon is OQY.

其他以 Cook Incorporated 為申請人之記錄

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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相關器械（代碼：OQY）

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。

K253642Jada系統（Jada-2002）Organon, LLC K230849ELLAVIDBTSinapi Biomedical (Pty) , Ltd.K212757Jada 系統Alydia Health K201199Jada 系統Alydia Health K191264每秒都重要-子宮內膜氣囊填塞術（“ESM-UBT”）Ujenzi Charitable Trust K170622巴克里產後氣球，巴克里產後氣球搭配快速注入元件Cook Incorporated

官方來源

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