Filbloc
K号: K150553 · 2016-05-19
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器械摘要
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.
常见问题
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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相关器械（代码：NEW）
关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。
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官方来源
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