oCare 腕式脉搏血氧仪
K号: K183556 · 2019-02-15
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器械摘要
常见问题
What is the oCare Wrist Pulse Oximeter?
oCare Wrist Pulse Oximeter is a medical device that received FDA 510(k) clearance on 2019-02-15. The listed applicant is Taiwan Biophotonic Corporation. The 510(k) number is K183556.
When did oCare Wrist Pulse Oximeter receive FDA 510(k) clearance?
oCare Wrist Pulse Oximeter received FDA 510(k) clearance on 2019-02-15, under 510(k) number K183556.
Who is the listed applicant for oCare Wrist Pulse Oximeter?
The FDA 510(k) record lists Taiwan Biophotonic Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for oCare Wrist Pulse Oximeter?
The FDA product code for oCare Wrist Pulse Oximeter is DQA.
相关临床试验
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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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