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FDA 510(k)

檸檬酸完整乾燥檸檬酸(45X)

K 號:K171750 · 2018-03-06

決定日期2018-03-06
產品代碼KPO
諮詢委員會GU
決定相當於

器材摘要

Citric Complete Dry Citric Acid (45X) is the device name listed in this FDA 510(k) record. The listed applicant is Dimesol USA, LLC. It received FDA 510(k) clearance on 2018-03-06 under 510(k) number K171750. The device is classified under product code KPO. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Citric Complete Dry Citric Acid (45X)?

Citric Complete Dry Citric Acid (45X) is a medical device that received FDA 510(k) clearance on 2018-03-06. The listed applicant is Dimesol USA, LLC. The 510(k) number is K171750.

When did Citric Complete Dry Citric Acid (45X) receive FDA 510(k) clearance?

Citric Complete Dry Citric Acid (45X) received FDA 510(k) clearance on 2018-03-06, under 510(k) number K171750.

Who is the listed applicant for Citric Complete Dry Citric Acid (45X)?

The FDA 510(k) record lists Dimesol USA, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Citric Complete Dry Citric Acid (45X)?

The FDA product code for Citric Complete Dry Citric Acid (45X) is KPO.

相關臨床試驗

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相關器械(代碼:KPO)

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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