Leadtek 指尖脉搏血氧仪
K号: K193350 · 2020-04-27
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器械摘要
常见问题
What is the Leadtek Fingertip Pulse Oximeter?
Leadtek Fingertip Pulse Oximeter is a medical device that received FDA 510(k) clearance on 2020-04-27. The listed applicant is Leadtek Research, Inc.. The 510(k) number is K193350.
When did Leadtek Fingertip Pulse Oximeter receive FDA 510(k) clearance?
Leadtek Fingertip Pulse Oximeter received FDA 510(k) clearance on 2020-04-27, under 510(k) number K193350.
Who is the listed applicant for Leadtek Fingertip Pulse Oximeter?
The FDA 510(k) record lists Leadtek Research, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Leadtek Fingertip Pulse Oximeter?
The FDA product code for Leadtek Fingertip Pulse Oximeter is DQA.
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Leadtek Research, 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:DQA)
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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