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FDA 510(k)

Anovo Surgical System (6Ne)

K 號:K250591 · 2025-06-06

決定日期2025-06-06
產品代碼QNM
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

Anovo Surgical System (6Ne) is the device name listed in this FDA 510(k) record. The listed applicant is Momentis Surgical , Ltd.. It received FDA 510(k) clearance on 2025-06-06 under 510(k) number K250591. The device is classified under product code QNM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Anovo Surgical System (6Ne)?

Anovo Surgical System (6Ne) is a medical device that received FDA 510(k) clearance on 2025-06-06. The listed applicant is Momentis Surgical , Ltd.. The 510(k) number is K250591.

When did Anovo Surgical System (6Ne) receive FDA 510(k) clearance?

Anovo Surgical System (6Ne) received FDA 510(k) clearance on 2025-06-06, under 510(k) number K250591.

Who is the listed applicant for Anovo Surgical System (6Ne)?

FDA 510(k) 記錄將 Momentis Surgical, Ltd. 列為申請人。這並不單獨確立設備製造商。

What is the FDA product code for Anovo Surgical System (6Ne)?

The FDA product code for Anovo Surgical System (6Ne) is QNM.

相關臨床試驗

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其他以 Momentis Surgical , Ltd. 為申請人之記錄

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相關器械(代碼:QNM)

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。

官方來源

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