Acumen 低血压预测指数,HemoSphere 高级监测平台
K号: K203224 · 2021-07-30
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器械摘要
常见问题
What is the Acumen Hypotension Prediction Index, HemoSphere Advanced Monitoring Platform?
Acumen Hypotension Prediction Index, HemoSphere Advanced Monitoring Platform is a medical device that received FDA 510(k) clearance on 2021-07-30. The listed applicant is Edwards Lifesciences, LLC. The 510(k) number is K203224.
When did Acumen Hypotension Prediction Index, HemoSphere Advanced Monitoring Platform receive FDA 510(k) clearance?
Acumen Hypotension Prediction Index, HemoSphere Advanced Monitoring Platform received FDA 510(k) clearance on 2021-07-30, under 510(k) number K203224.
Who is the listed applicant for Acumen Hypotension Prediction Index, HemoSphere Advanced Monitoring Platform?
The FDA 510(k) record lists Edwards Lifesciences, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Acumen Hypotension Prediction Index, HemoSphere Advanced Monitoring Platform?
The FDA product code for Acumen Hypotension Prediction Index, HemoSphere Advanced Monitoring Platform is QAQ.
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Edwards Lifesciences, 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:QAQ)
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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