再生处理诊断超声导管
K号: K153090 · 2016-03-10
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器械摘要
常见问题
What is the Reprocessed Diagnostic Ultrasound Catheter?
Reprocessed Diagnostic Ultrasound Catheter is a medical device that received FDA 510(k) clearance on 2016-03-10. The listed applicant is Innovative Health, LLC. The 510(k) number is K153090.
When did Reprocessed Diagnostic Ultrasound Catheter receive FDA 510(k) clearance?
Reprocessed Diagnostic Ultrasound Catheter received FDA 510(k) clearance on 2016-03-10, under 510(k) number K153090.
Who is the listed applicant for Reprocessed Diagnostic Ultrasound Catheter?
The FDA 510(k) record lists Innovative Health, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Reprocessed Diagnostic Ultrasound Catheter?
The FDA product code for Reprocessed Diagnostic Ultrasound Catheter is OWQ.
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Innovative Health, LLC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:OWQ)
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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