MaxZero 扩展组件带无需连接器
K号: K171957 · 2017-07-19
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器械摘要
常见问题
What is the MaxZero Extension Sets with Needless Connector?
MaxZero Extension Sets with Needless Connector is a medical device that received FDA 510(k) clearance on 2017-07-19. The listed applicant is Carefusion 303, Inc.. The 510(k) number is K171957.
When did MaxZero Extension Sets with Needless Connector receive FDA 510(k) clearance?
MaxZero Extension Sets with Needless Connector received FDA 510(k) clearance on 2017-07-19, under 510(k) number K171957.
Who is the listed applicant for MaxZero Extension Sets with Needless Connector?
The FDA 510(k) record lists Carefusion 303, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MaxZero Extension Sets with Needless Connector?
The FDA product code for MaxZero Extension Sets with Needless Connector is FPA.
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。
列明Carefusion 303, Inc.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:FPA)
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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