FDA 510(k)

ANNE 妇科

K 號：K253021 · 2026-02-26

決定日期2026-02-26

產品代碼HGM

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

ANNE Maternal is the device name listed in this FDA 510(k) record. The listed applicant is Sibel Health, Inc.. It received FDA 510(k) clearance on 2026-02-26 under 510(k) number K253021. The device is classified under product code HGM. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the ANNE Maternal?

ANNE Maternal is a medical device that received FDA 510(k) clearance on 2026-02-26. The listed applicant is Sibel Health, Inc.. The 510(k) number is K253021.

When did ANNE Maternal receive FDA 510(k) clearance?

ANNE Maternal received FDA 510(k) clearance on 2026-02-26, under 510(k) number K253021.

Who is the listed applicant for ANNE Maternal?

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

What is the FDA product code for ANNE Maternal?

The FDA product code for ANNE Maternal is HGM.

其他以 Sibel Health, Inc. 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。

K242842ANNE View, 中央樞紐 K240251ANNE 胸部 K240305ANNE 四肢 K223711ANNE 一體

相關器械（代碼：HGM）

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。

K254036Novii+ 電子貼片系統Datex Ohmeda, Inc.K250777Sonicaid Team3Huntleigh Healthcare , Ltd.K241882胎兒及母親監護器（F15A，F15A Air）Edan Instruments, Inc.K241368Sonicaid Team3Huntleigh Healthcare , Ltd.K241009PeriCALM 模式 3.0Perigen, Inc.K233440Avalon CL 胎兒與母親 (F&M) Pod (866488)，Avalon CL 胎兒與母親 (F&M) 贴片 (989803196341)Philips Medizin Systeme Boeblingen GmbH

官方來源

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