FDA 510(k)

光刀配煙氣抽離功能

K 號：K191583 · 2020-03-06

決定日期2020-03-06

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

PhotonBlade with Smoke Evacuation is the device name listed in this FDA 510(k) record. The listed applicant is Invuity, Inc.. It received FDA 510(k) clearance on 2020-03-06 under 510(k) number K191583. 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 PhotonBlade with Smoke Evacuation?

PhotonBlade with Smoke Evacuation is a medical device that received FDA 510(k) clearance on 2020-03-06. The listed applicant is Invuity, Inc.. The 510(k) number is K191583.

When did PhotonBlade with Smoke Evacuation receive FDA 510(k) clearance?

PhotonBlade with Smoke Evacuation received FDA 510(k) clearance on 2020-03-06, under 510(k) number K191583.

Who is the listed applicant for PhotonBlade with Smoke Evacuation?

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

What is the FDA product code for PhotonBlade with Smoke Evacuation?

The FDA product code for PhotonBlade with Smoke Evacuation is GEI.

其他以 Invuity, 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。

K162053光子刀

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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官方來源

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