FDA 510(k)

Servator B 輔助溶液

K 號：K180481 · 2018-06-29

決定日期2018-06-29

產品代碼KDN

諮詢委員會GU

決定相當於

器材摘要

Servator B SALF Solution is the device name listed in this FDA 510(k) record. The listed applicant is S.A.L.F. Spa. It received FDA 510(k) clearance on 2018-06-29 under 510(k) number K180481. The device is classified under product code KDN. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Servator B SALF Solution?

Servator B SALF Solution is a medical device that received FDA 510(k) clearance on 2018-06-29. The listed applicant is S.A.L.F. Spa. The 510(k) number is K180481.

When did Servator B SALF Solution receive FDA 510(k) clearance?

Servator B SALF Solution received FDA 510(k) clearance on 2018-06-29, under 510(k) number K180481.

Who is the listed applicant for Servator B SALF Solution?

The FDA 510(k) record lists S.A.L.F. Spa as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Servator B SALF Solution?

The FDA product code for Servator B SALF Solution is KDN.

其他以 S.A.L.F. Spa 為申請人之記錄

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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相關器械（代碼：KDN）

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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