脉搏血氧仪(型号OHT60,OXH78)
K号: K230277 · 2024-01-04
广告
器械摘要
常见问题
What is the Pulse Oximeter(Model OHT60,OXH78)?
Pulse Oximeter(Model OHT60,OXH78) is a medical device that received FDA 510(k) clearance on 2024-01-04. The listed applicant is Cofoe Medical Technology Co., Ltd.. The 510(k) number is K230277.
When did Pulse Oximeter(Model OHT60,OXH78) receive FDA 510(k) clearance?
Pulse Oximeter(Model OHT60,OXH78) received FDA 510(k) clearance on 2024-01-04, under 510(k) number K230277.
Who is the listed applicant for Pulse Oximeter(Model OHT60,OXH78)?
The FDA 510(k) record lists Cofoe Medical Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Pulse Oximeter(Model OHT60,OXH78)?
The FDA product code for Pulse Oximeter(Model OHT60,OXH78) 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。
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。
广告