Quantumn 中心血泵驱动-高压, Quantumn 中心血泵驱动-中压
K号: K192838 · 2020-04-13
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器械摘要
常见问题
What is the Quantumn Centrifugal Drive- High Pressure, Quantum Centrifugal Drive- Medium Pressure?
Quantumn Centrifugal Drive- High Pressure, Quantum Centrifugal Drive- Medium Pressure is a medical device that received FDA 510(k) clearance on 2020-04-13. The listed applicant is Spectrum Medical , Ltd.. The 510(k) number is K192838.
When did Quantumn Centrifugal Drive- High Pressure, Quantum Centrifugal Drive- Medium Pressure receive FDA 510(k) clearance?
Quantumn Centrifugal Drive- High Pressure, Quantum Centrifugal Drive- Medium Pressure received FDA 510(k) clearance on 2020-04-13, under 510(k) number K192838.
Who is the listed applicant for Quantumn Centrifugal Drive- High Pressure, Quantum Centrifugal Drive- Medium Pressure?
The FDA 510(k) record lists Spectrum Medical , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Quantumn Centrifugal Drive- High Pressure, Quantum Centrifugal Drive- Medium Pressure?
The FDA product code for Quantumn Centrifugal Drive- High Pressure, Quantum Centrifugal Drive- Medium Pressure is DWA.
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Spectrum Medical , Ltd.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:DWA)
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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