手指血氧計
K 號：K163135 · 2017-09-19
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器材摘要
Finger Pulse Oximeter is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Fitfaith Technology Co.,Ltd. It received FDA 510(k) clearance on 2017-09-19 under 510(k) number K163135. The device is classified under product code DQA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Finger Pulse Oximeter?
Finger Pulse Oximeter is a medical device that received FDA 510(k) clearance on 2017-09-19. The listed applicant is Shenzhen Fitfaith Technology Co.,Ltd. The 510(k) number is K163135.
When did Finger Pulse Oximeter receive FDA 510(k) clearance?
Finger Pulse Oximeter received FDA 510(k) clearance on 2017-09-19, under 510(k) number K163135.
Who is the listed applicant for Finger Pulse Oximeter?
The FDA 510(k) record lists Shenzhen Fitfaith Technology Co.,Ltd as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Finger Pulse Oximeter?
The FDA product code for Finger Pulse Oximeter is DQA.
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相關器械（代碼：DQA）
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。
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官方來源
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