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FDA 510(k)

da Vinci X/Xi 8mm內視鏡加強版,0,da Vinci X/Xi 8mm內視鏡加強版,30

K 號:K191736 · 2019-07-26

決定日期2019-07-26
產品代碼NAY
諮詢委員會GU
決定相當於

器材摘要

da Vinci X/Xi 8mm Endoscope Plus, 0, da Vinci X/Xi 8mm Endoscope Plus, 30 is the device name listed in this FDA 510(k) record. The listed applicant is Intuitive Surgical. It received FDA 510(k) clearance on 2019-07-26 under 510(k) number K191736. 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 X/Xi 8mm Endoscope Plus, 0, da Vinci X/Xi 8mm Endoscope Plus, 30?

da Vinci X/Xi 8mm Endoscope Plus, 0, da Vinci X/Xi 8mm Endoscope Plus, 30 is a medical device that received FDA 510(k) clearance on 2019-07-26. The listed applicant is Intuitive Surgical. The 510(k) number is K191736.

When did da Vinci X/Xi 8mm Endoscope Plus, 0, da Vinci X/Xi 8mm Endoscope Plus, 30 receive FDA 510(k) clearance?

da Vinci X/Xi 8mm Endoscope Plus, 0, da Vinci X/Xi 8mm Endoscope Plus, 30 received FDA 510(k) clearance on 2019-07-26, under 510(k) number K191736.

Who is the listed applicant for da Vinci X/Xi 8mm Endoscope Plus, 0, da Vinci X/Xi 8mm Endoscope Plus, 30?

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

What is the FDA product code for da Vinci X/Xi 8mm Endoscope Plus, 0, da Vinci X/Xi 8mm Endoscope Plus, 30?

The FDA product code for da Vinci X/Xi 8mm Endoscope Plus, 0, da Vinci X/Xi 8mm Endoscope Plus, 30 is NAY.

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其他以 Intuitive Surgical 為申請人之記錄

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相關器械(代碼:NAY)

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