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FDA 510(k)

LCCS VC-S RF Cannula

K 號:K191293 · 2020-01-24

決定日期2020-01-24
產品代碼GXI
諮詢委員會NE (請提供完整的英文描述,以便進行翻譯。)
決定相當於

器材摘要

LCCS VC-S RF Cannula is the device name listed in this FDA 510(k) record. The listed applicant is Lccs Products Limited. It received FDA 510(k) clearance on 2020-01-24 under 510(k) number K191293. The device is classified under product code GXI. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the LCCS VC-S RF Cannula?

LCCS VC-S RF Cannula is a medical device that received FDA 510(k) clearance on 2020-01-24. The listed applicant is Lccs Products Limited. The 510(k) number is K191293.

When did LCCS VC-S RF Cannula receive FDA 510(k) clearance?

LCCS VC-S RF Cannula received FDA 510(k) clearance on 2020-01-24, under 510(k) number K191293.

Who is the listed applicant for LCCS VC-S RF Cannula?

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

What is the FDA product code for LCCS VC-S RF Cannula?

The FDA product code for LCCS VC-S RF Cannula is GXI.

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。

其他以 Lccs Products Limited 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。

相關器械(代碼:GXI)

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。

官方來源

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