QUANTIEN測量系統
K 號：K172182 · 2017-08-18
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器材摘要
QUANTIEN Measurement System is the device name listed in this FDA 510(k) record. The listed applicant is St. Jude Medical (Now Part of the Abbott Medical). It received FDA 510(k) clearance on 2017-08-18 under 510(k) number K172182. The device is classified under product code DQK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the QUANTIEN Measurement System?
QUANTIEN Measurement System is a medical device that received FDA 510(k) clearance on 2017-08-18. The listed applicant is St. Jude Medical (Now Part of the Abbott Medical). The 510(k) number is K172182.
When did QUANTIEN Measurement System receive FDA 510(k) clearance?
QUANTIEN Measurement System received FDA 510(k) clearance on 2017-08-18, under 510(k) number K172182.
Who is the listed applicant for QUANTIEN Measurement System?
The FDA 510(k) record lists St. Jude Medical (Now Part of the Abbott Medical) as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for QUANTIEN Measurement System?
The FDA product code for QUANTIEN Measurement System is DQK.
相關臨床試驗
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相關器械（代碼：DQK）
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
在 FDA 資料庫中查看 →資料來源為 FDA Open API。如需最新且權威的資訊，請始終參閱官方記錄。
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