CareView 1800Le
K号: K193173 · 2019-12-13
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器械摘要
CareView 1800Le is the device name listed in this FDA 510(k) record. The listed applicant is Careray Digital Medical System Co., Ltd.. It received FDA 510(k) clearance on 2019-12-13 under 510(k) number K193173. The device is classified under product code MQB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the CareView 1800Le?
CareView 1800Le is a medical device that received FDA 510(k) clearance on 2019-12-13. The listed applicant is Careray Digital Medical System Co., Ltd.. The 510(k) number is K193173.
When did CareView 1800Le receive FDA 510(k) clearance?
CareView 1800Le received FDA 510(k) clearance on 2019-12-13, under 510(k) number K193173.
Who is the listed applicant for CareView 1800Le?
The FDA 510(k) record lists Careray Digital Medical System Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CareView 1800Le?
The FDA product code for CareView 1800Le is MQB.
相关临床试验
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列明Careray Digital Medical System 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：MQB）
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。
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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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