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FDA 510(k)

視覺器(5.4);元素視覺器;混合現實視覺器;智慧佈局;元素視覺器智慧佈局

K 號:K232759 · 2024-05-21

申請人Brainlab AG
決定日期2024-05-21
產品代碼LLZ
諮詢委員會RA
決定相當於

器材摘要

Viewer (5.4); Elements Viewer; Mixed Reality Viewer; Smart Layout; Elements Viewer Smart Layout is the device name listed in this FDA 510(k) record. The listed applicant is Brainlab AG. It received FDA 510(k) clearance on 2024-05-21 under 510(k) number K232759. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Viewer (5.4); Elements Viewer; Mixed Reality Viewer; Smart Layout; Elements Viewer Smart Layout?

Viewer (5.4); Elements Viewer; Mixed Reality Viewer; Smart Layout; Elements Viewer Smart Layout is a medical device that received FDA 510(k) clearance on 2024-05-21. The listed applicant is Brainlab AG. The 510(k) number is K232759.

When did Viewer (5.4); Elements Viewer; Mixed Reality Viewer; Smart Layout; Elements Viewer Smart Layout receive FDA 510(k) clearance?

Viewer (5.4); Elements Viewer; Mixed Reality Viewer; Smart Layout; Elements Viewer Smart Layout received FDA 510(k) clearance on 2024-05-21, under 510(k) number K232759.

Who is the listed applicant for Viewer (5.4); Elements Viewer; Mixed Reality Viewer; Smart Layout; Elements Viewer Smart Layout?

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

What is the FDA product code for Viewer (5.4); Elements Viewer; Mixed Reality Viewer; Smart Layout; Elements Viewer Smart Layout?

The FDA product code for Viewer (5.4); Elements Viewer; Mixed Reality Viewer; Smart Layout; Elements Viewer Smart Layout is LLZ.

相關臨床試驗

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其他以 Brainlab AG 為申請人之記錄

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相關器械(代碼:LLZ)

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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