手持式脉搏血氧仪
K号: K213431 · 2023-02-26
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器械摘要
常见问题
What is the Handheld Pulse Oximeter?
Handheld Pulse Oximeter is a medical device that received FDA 510(k) clearance on 2023-02-26. The listed applicant is Shenzhen Witleaf Medical Electronics Co., Ltd.. The 510(k) number is K213431.
When did Handheld Pulse Oximeter receive FDA 510(k) clearance?
Handheld Pulse Oximeter received FDA 510(k) clearance on 2023-02-26, under 510(k) number K213431.
Who is the listed applicant for Handheld Pulse Oximeter?
The FDA 510(k) record lists Shenzhen Witleaf Medical Electronics Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Handheld Pulse Oximeter?
The FDA product code for Handheld 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Shenzhen Witleaf Medical Electronics Co., 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: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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