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FDA 510(k)

微波消融系統

K 號:K183153 · 2019-07-08

決定日期2019-07-08
產品代碼NEY
諮詢委員會SU 請提供完整的描述文本,以便我進行翻譯。
決定相當於

器材摘要

Microwave Ablation System is the device name listed in this FDA 510(k) record. The listed applicant is Surgnova Healthcare Technologies (Zhejiang) Co., Ltd.. It received FDA 510(k) clearance on 2019-07-08 under 510(k) number K183153. The device is classified under product code NEY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Microwave Ablation System?

Microwave Ablation System is a medical device that received FDA 510(k) clearance on 2019-07-08. The listed applicant is Surgnova Healthcare Technologies (Zhejiang) Co., Ltd.. The 510(k) number is K183153.

When did Microwave Ablation System receive FDA 510(k) clearance?

Microwave Ablation System received FDA 510(k) clearance on 2019-07-08, under 510(k) number K183153.

Who is the listed applicant for Microwave Ablation System?

The FDA 510(k) record lists Surgnova Healthcare Technologies (Zhejiang) Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Microwave Ablation System?

The FDA product code for Microwave Ablation System is NEY.

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其他以 Surgnova Healthcare Technologies (Zhejiang) Co., Ltd. 為申請人之記錄

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相關器械(代碼:NEY)

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