OC-FLEX 強柔內口腔管
K 號：K161250 · 2017-03-17
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器材摘要
OC-FLEX Flexible IntraOral Cannula is the device name listed in this FDA 510(k) record. The listed applicant is Venture Therapeutics, Inc.. It received FDA 510(k) clearance on 2017-03-17 under 510(k) number K161250. The device is classified under product code CCK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the OC-FLEX Flexible IntraOral Cannula?
OC-FLEX Flexible IntraOral Cannula is a medical device that received FDA 510(k) clearance on 2017-03-17. The listed applicant is Venture Therapeutics, Inc.. The 510(k) number is K161250.
When did OC-FLEX Flexible IntraOral Cannula receive FDA 510(k) clearance?
OC-FLEX Flexible IntraOral Cannula received FDA 510(k) clearance on 2017-03-17, under 510(k) number K161250.
Who is the listed applicant for OC-FLEX Flexible IntraOral Cannula?
The FDA 510(k) record lists Venture Therapeutics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OC-FLEX Flexible IntraOral Cannula?
The FDA product code for OC-FLEX Flexible IntraOral Cannula is CCK.
相關臨床試驗
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相關器械（代碼：CCK）
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。
K251641GF-310R 多氣體單元（GF-310R）Nihon Kohden CorporationK261633視覺呼吸Affirm Medical Technologies II, LLCK253030Capnostream™35 輕便呼吸監測器 (PM35MN)Covidien, LLCK250148醫療氣體分析儀（AG200）Prior Care Science Technology, Ltd.K243956TG-980P 二氧化碳感測器套件（TG-980P）；TG-980P1 二氧化碳感測器套件（TG-980P1）Nihon Kohden CorporationK2512160184 CO2 標本採集管；0184T CO2 標本採集管；0139 CO2 標本採集管；0182 CO2 標本採集管Barbaras Development, Inc.
官方來源
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