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FDA 510(k)

Active Needle Endoscopic Treatment (ANET) 電外科應用器

K 號：K170990 · 2017-05-11

申請人Spiration, Inc.
決定日期2017-05-11
產品代碼GEI
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

Active Needle Endoscopic Treatment (ANET) Electrosurgical Applicator is the device name listed in this FDA 510(k) record. The listed applicant is Spiration, Inc.. It received FDA 510(k) clearance on 2017-05-11 under 510(k) number K170990. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Active Needle Endoscopic Treatment (ANET) Electrosurgical Applicator?

Active Needle Endoscopic Treatment (ANET) Electrosurgical Applicator is a medical device that received FDA 510(k) clearance on 2017-05-11. The listed applicant is Spiration, Inc.. The 510(k) number is K170990.

When did Active Needle Endoscopic Treatment (ANET) Electrosurgical Applicator receive FDA 510(k) clearance?

Active Needle Endoscopic Treatment (ANET) Electrosurgical Applicator received FDA 510(k) clearance on 2017-05-11, under 510(k) number K170990.

Who is the listed applicant for Active Needle Endoscopic Treatment (ANET) Electrosurgical Applicator?

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

What is the FDA product code for Active Needle Endoscopic Treatment (ANET) Electrosurgical Applicator?

The FDA product code for Active Needle Endoscopic Treatment (ANET) Electrosurgical Applicator is GEI.

相關臨床試驗

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。

NCT07608549FLASH 預試階段 1 安全性研究NOT_YET_RECRUITINGNCT06562205PAP系統外部臨床研究（ECS）NOT_YET_RECRUITINGNCT06443177對於動脈瘤性硬腦膜下出血引起的腦血管收縮，交感調節的影響SUSPENDEDNCT07095751人工智能協助的Uro-Cam導尿管評估系統，用於診斷膀胱癌NOT_YET_RECRUITING

其他以 Spiration, 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。

K171492B7 2C 閉塞氣球K162611PeriFLEXK152922ViziShot FLEX

相關器械（代碼：GEI）

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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