FDA 510(k)

達芬奇單點儀器及附件

K 號：K152448 · 2016-03-09

決定日期2016-03-09

產品代碼NAY

諮詢委員會GU

決定相當於

器材摘要

da Vinci Single-Site Instrument and Accessories 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 2016-03-09 under 510(k) number K152448. 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 Single-Site Instrument and Accessories?

da Vinci Single-Site Instrument and Accessories is a medical device that received FDA 510(k) clearance on 2016-03-09. The listed applicant is Intuitive Surgical, Inc.. The 510(k) number is K152448.

When did da Vinci Single-Site Instrument and Accessories receive FDA 510(k) clearance?

da Vinci Single-Site Instrument and Accessories received FDA 510(k) clearance on 2016-03-09, under 510(k) number K152448.

Who is the listed applicant for da Vinci Single-Site Instrument and Accessories?

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 Single-Site Instrument and Accessories?

The FDA product code for da Vinci Single-Site Instrument and Accessories is NAY.

其他以 Intuitive Surgical, 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。

K261823達芬奇手術系統，型號IS5000 K253702直觀內腔結腸胃腸系統（IG1000）K261824達芬奇手術系統，型號IS5000 K261249通用密封 (5-12 毫米)K253986da Vinci Force Feedback Instruments K253978通用密封 (5-12 毫米)

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相關器械（代碼：NAY）

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。

K261823達芬奇手術系統，型號IS5000Intuitive Surgical, Inc.K261824達芬奇手術系統，型號IS5000Intuitive Surgical, Inc.K260695達芬奇火飛行影響系統Intuitive Surgical K254192昇強超聲波系統Asensus Surgical K253986da Vinci Force Feedback InstrumentsIntuitive Surgical, Inc.K253556達芬奇SP外科系統（SP1098）；達芬奇E-200發生器Intuitive Surgical, Inc.

官方來源

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