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FDA 510(k)

AquaShield 系統 - PENTAX, AquaShield 系統 CO2 - PENTAX, AquaShield 系統 CO2 - FUJINON

K 號:K163424 · 2017-01-04

決定日期2017-01-04
產品代碼FEQ
諮詢委員會GU
決定相當於

器材摘要

AquaShield System - PENTAX, AquaShield System CO2 - PENTAX, AquaShield System CO2 - FUJINON is the device name listed in this FDA 510(k) record. The listed applicant is United State Endoscopy Group, Inc.. It received FDA 510(k) clearance on 2017-01-04 under 510(k) number K163424. The device is classified under product code FEQ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the AquaShield System - PENTAX, AquaShield System CO2 - PENTAX, AquaShield System CO2 - FUJINON?

AquaShield System - PENTAX, AquaShield System CO2 - PENTAX, AquaShield System CO2 - FUJINON is a medical device that received FDA 510(k) clearance on 2017-01-04. The listed applicant is United State Endoscopy Group, Inc.. The 510(k) number is K163424.

When did AquaShield System - PENTAX, AquaShield System CO2 - PENTAX, AquaShield System CO2 - FUJINON receive FDA 510(k) clearance?

AquaShield System - PENTAX, AquaShield System CO2 - PENTAX, AquaShield System CO2 - FUJINON received FDA 510(k) clearance on 2017-01-04, under 510(k) number K163424.

Who is the listed applicant for AquaShield System - PENTAX, AquaShield System CO2 - PENTAX, AquaShield System CO2 - FUJINON?

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

What is the FDA product code for AquaShield System - PENTAX, AquaShield System CO2 - PENTAX, AquaShield System CO2 - FUJINON?

The FDA product code for AquaShield System - PENTAX, AquaShield System CO2 - PENTAX, AquaShield System CO2 - FUJINON is FEQ.

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。

相關器械(代碼:FEQ)

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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