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FDA 510(k)

達芬奇SP外科系統(SP1098);達芬奇E-200發生器

K 號:K253556 · 2026-01-16

決定日期2026-01-16
產品代碼NAY
諮詢委員會GU
決定相當於

器材摘要

da Vinci SP Surgical System (SP1098); da Vinci E-200 Generator is the device name listed in this FDA 510(k) record. The listed applicant is Intuitive Surgical, Inc.. It received FDA 510(k) clearance on 2026-01-16 under 510(k) number K253556. The device is classified under product code NAY. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the da Vinci SP Surgical System (SP1098); da Vinci E-200 Generator?

da Vinci SP Surgical System (SP1098); da Vinci E-200 Generator is a medical device that received FDA 510(k) clearance on 2026-01-16. The listed applicant is Intuitive Surgical, Inc.. The 510(k) number is K253556.

When did da Vinci SP Surgical System (SP1098); da Vinci E-200 Generator receive FDA 510(k) clearance?

da Vinci SP Surgical System (SP1098); da Vinci E-200 Generator received FDA 510(k) clearance on 2026-01-16, under 510(k) number K253556.

Who is the listed applicant for da Vinci SP Surgical System (SP1098); da Vinci E-200 Generator?

FDA 510(k) 記錄將 Intuitive Surgical, 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 da Vinci SP Surgical System (SP1098); da Vinci E-200 Generator?

The FDA product code for da Vinci SP Surgical System (SP1098); da Vinci E-200 Generator is NAY.

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其他以 Intuitive Surgical, Inc. 為申請人之記錄

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相關器械(代碼:NAY)

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官方來源

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