Cantab Mobile
K 號：K161328 · 2017-01-13
廣告
決定日期2017-01-13
產品代碼PKQ
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
Cantab Mobile is the device name listed in this FDA 510(k) record. The listed applicant is Cambridge Cognition , Ltd., US Agent: Clementi Associates , Ltd.. It received FDA 510(k) clearance on 2017-01-13 under 510(k) number K161328. The device is classified under product code PKQ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Cantab Mobile?
Cantab Mobile is a medical device that received FDA 510(k) clearance on 2017-01-13. The listed applicant is Cambridge Cognition , Ltd., US Agent: Clementi Associates , Ltd.. The 510(k) number is K161328.
When did Cantab Mobile receive FDA 510(k) clearance?
Cantab Mobile received FDA 510(k) clearance on 2017-01-13, under 510(k) number K161328.
Who is the listed applicant for Cantab Mobile?
The FDA 510(k) record lists Cambridge Cognition , Ltd., US Agent: Clementi Associates , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Cantab Mobile?
The FDA product code for Cantab Mobile is PKQ.
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官方來源
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