Filbloc
K 號：K150553 · 2016-05-19
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器材摘要
Filbloc is the device name listed in this FDA 510(k) record. The listed applicant is Assut Europe. It received FDA 510(k) clearance on 2016-05-19 under 510(k) number K150553. The device is classified under product code NEW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Filbloc?
Filbloc is a medical device that received FDA 510(k) clearance on 2016-05-19. The listed applicant is Assut Europe. The 510(k) number is K150553.
When did Filbloc receive FDA 510(k) clearance?
Filbloc received FDA 510(k) clearance on 2016-05-19, under 510(k) number K150553.
Who is the listed applicant for Filbloc?
The FDA 510(k) record lists Assut Europe as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Filbloc?
The FDA product code for Filbloc is NEW.
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相關器械（代碼：NEW）
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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