Accurate Mini非侵入式血压监测仪(AMB-001)。
K号: K242352 · 2025-02-05
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器械摘要
常见问题
What is the Accurate Mini Non-invasive blood pressure monitor (AMB-001)?
Accurate Mini Non-invasive blood pressure monitor (AMB-001) is a medical device that received FDA 510(k) clearance on 2025-02-05. The listed applicant is Accurate Meditech, Inc.. The 510(k) number is K242352.
When did Accurate Mini Non-invasive blood pressure monitor (AMB-001) receive FDA 510(k) clearance?
Accurate Mini Non-invasive blood pressure monitor (AMB-001) received FDA 510(k) clearance on 2025-02-05, under 510(k) number K242352.
Who is the listed applicant for Accurate Mini Non-invasive blood pressure monitor (AMB-001)?
The FDA 510(k) record lists Accurate Meditech, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Accurate Mini Non-invasive blood pressure monitor (AMB-001)?
The FDA product code for Accurate Mini Non-invasive blood pressure monitor (AMB-001) is DXN.
相关临床试验
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列明Accurate Meditech, 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:DXN)
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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