Clearum HS 系列,Clearum HS 型号:HS 13, HS 15, HS 17, HS 20, HS 22
K号: K193542 · 2020-10-08
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器械摘要
常见问题
What is the Clearum HS Family, Clearum HS Models: HS 13, HS 15, HS 17, HS 20, HS 22?
Clearum HS Family, Clearum HS Models: HS 13, HS 15, HS 17, HS 20, HS 22 is a medical device that received FDA 510(k) clearance on 2020-10-08. The listed applicant is Bellco Srl. The 510(k) number is K193542.
When did Clearum HS Family, Clearum HS Models: HS 13, HS 15, HS 17, HS 20, HS 22 receive FDA 510(k) clearance?
Clearum HS Family, Clearum HS Models: HS 13, HS 15, HS 17, HS 20, HS 22 received FDA 510(k) clearance on 2020-10-08, under 510(k) number K193542.
Who is the listed applicant for Clearum HS Family, Clearum HS Models: HS 13, HS 15, HS 17, HS 20, HS 22?
The FDA 510(k) record lists Bellco Srl as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Clearum HS Family, Clearum HS Models: HS 13, HS 15, HS 17, HS 20, HS 22?
The FDA product code for Clearum HS Family, Clearum HS Models: HS 13, HS 15, HS 17, HS 20, HS 22 is KDI.
相关临床试验
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列明Bellco Srl为申报人的其他记录
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。
相关器械(代码:KDI)
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。
官方来源
在 FDA 数据库中查看 →数据来源于FDA开放API。如需最新且权威的信息,请务必参考官方记录。
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