RAYSCAN a-Expert3D
K号: K190812 · 2019-04-24
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器械摘要
RAYSCAN a-Expert3D is the device name listed in this FDA 510(k) record. The listed applicant is Ray Co., Ltd.. It received FDA 510(k) clearance on 2019-04-24 under 510(k) number K190812. The device is classified under product code OAS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the RAYSCAN a-Expert3D?
RAYSCAN a-Expert3D is a medical device that received FDA 510(k) clearance on 2019-04-24. The listed applicant is Ray Co., Ltd.. The 510(k) number is K190812.
When did RAYSCAN a-Expert3D receive FDA 510(k) clearance?
RAYSCAN a-Expert3D received FDA 510(k) clearance on 2019-04-24, under 510(k) number K190812.
Who is the listed applicant for RAYSCAN a-Expert3D?
The FDA 510(k) record lists Ray Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RAYSCAN a-Expert3D?
The FDA product code for RAYSCAN a-Expert3D is OAS.
相关临床试验
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列明Ray 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：OAS）
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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