Avantgarde粪便管理系统,Avantgarde粪便管理系统更换袋
K号: K193325 · 2020-03-13
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器械摘要
常见问题
What is the Avantgarde Faecal Management Systems, Avantgarde Faecal Management System Replacement Pouches?
Avantgarde Faecal Management Systems, Avantgarde Faecal Management System Replacement Pouches is a medical device that received FDA 510(k) clearance on 2020-03-13. The listed applicant is Prosys International, Ltd.. The 510(k) number is K193325.
When did Avantgarde Faecal Management Systems, Avantgarde Faecal Management System Replacement Pouches receive FDA 510(k) clearance?
Avantgarde Faecal Management Systems, Avantgarde Faecal Management System Replacement Pouches received FDA 510(k) clearance on 2020-03-13, under 510(k) number K193325.
Who is the listed applicant for Avantgarde Faecal Management Systems, Avantgarde Faecal Management System Replacement Pouches?
The FDA 510(k) record lists Prosys International, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Avantgarde Faecal Management Systems, Avantgarde Faecal Management System Replacement Pouches?
The FDA product code for Avantgarde Faecal Management Systems, Avantgarde Faecal Management System Replacement Pouches is KNT.
相关临床试验
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:KNT)
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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