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FDA 510(k)

INTRACEPT柔軟雙極RF探針及易於存取工具組

K 號:K153272 · 2016-07-09

決定日期2016-07-09
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

INTRACEPT Flexible Bi-Polar RF Probe and Easy Access Instrument Set is the device name listed in this FDA 510(k) record. The listed applicant is Relievant Medsystems. It received FDA 510(k) clearance on 2016-07-09 under 510(k) number K153272. 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 INTRACEPT Flexible Bi-Polar RF Probe and Easy Access Instrument Set?

INTRACEPT Flexible Bi-Polar RF Probe and Easy Access Instrument Set is a medical device that received FDA 510(k) clearance on 2016-07-09. The listed applicant is Relievant Medsystems. The 510(k) number is K153272.

When did INTRACEPT Flexible Bi-Polar RF Probe and Easy Access Instrument Set receive FDA 510(k) clearance?

INTRACEPT Flexible Bi-Polar RF Probe and Easy Access Instrument Set received FDA 510(k) clearance on 2016-07-09, under 510(k) number K153272.

Who is the listed applicant for INTRACEPT Flexible Bi-Polar RF Probe and Easy Access Instrument Set?

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

What is the FDA product code for INTRACEPT Flexible Bi-Polar RF Probe and Easy Access Instrument Set?

The FDA product code for INTRACEPT Flexible Bi-Polar RF Probe and Easy Access Instrument Set is GXI.

相關臨床試驗

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其他以 Relievant Medsystems 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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