FDA 510(k)

維薩利周邊系統

K 號：K251312 · 2025-10-24

決定日期2025-10-24

產品代碼QEZ

諮詢委員會履歷

決定相當於

器材摘要

Vesalio Peripheral System is the device name listed in this FDA 510(k) record. The listed applicant is Vesalio, Inc.. It received FDA 510(k) clearance on 2025-10-24 under 510(k) number K251312. The device is classified under product code QEZ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Vesalio Peripheral System?

Vesalio Peripheral System is a medical device that received FDA 510(k) clearance on 2025-10-24. The listed applicant is Vesalio, Inc.. The 510(k) number is K251312.

When did Vesalio Peripheral System receive FDA 510(k) clearance?

Vesalio Peripheral System received FDA 510(k) clearance on 2025-10-24, under 510(k) number K251312.

Who is the listed applicant for Vesalio Peripheral System?

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

What is the FDA product code for Vesalio Peripheral System?

The FDA product code for Vesalio Peripheral System is QEZ.

其他以 Vesalio, 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：QEZ）

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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