FDA 510(k)

InbellaMulti 系統

K 號：K252367 · 2025-10-15

決定日期2025-10-15

產品代碼GEI

諮詢委員會SU 請提供完整的描述文本，以便我進行翻譯。

決定相當於

器材摘要

InbellaMulti System is the device name listed in this FDA 510(k) record. The listed applicant is Inbella Medical, Inc.. It received FDA 510(k) clearance on 2025-10-15 under 510(k) number K252367. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the InbellaMulti System?

InbellaMulti System is a medical device that received FDA 510(k) clearance on 2025-10-15. The listed applicant is Inbella Medical, Inc.. The 510(k) number is K252367.

When did InbellaMulti System receive FDA 510(k) clearance?

InbellaMulti System received FDA 510(k) clearance on 2025-10-15, under 510(k) number K252367.

Who is the listed applicant for InbellaMulti System?

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

What is the FDA product code for InbellaMulti System?

The FDA product code for InbellaMulti System is GEI.

其他以 Inbella Medical, 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。

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相關器械（代碼：GEI）

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

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