1417WCC_127um 和 1417WCC_140um
K号: K171418 · 2017-06-12
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器械摘要
1417WCC_127um and1417WCC_140um is the device name listed in this FDA 510(k) record. The listed applicant is Rayence Co., Ltd.. It received FDA 510(k) clearance on 2017-06-12 under 510(k) number K171418. 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 1417WCC_127um and1417WCC_140um?
1417WCC_127um and1417WCC_140um is a medical device that received FDA 510(k) clearance on 2017-06-12. The listed applicant is Rayence Co., Ltd.. The 510(k) number is K171418.
When did 1417WCC_127um and1417WCC_140um receive FDA 510(k) clearance?
1417WCC_127um and1417WCC_140um received FDA 510(k) clearance on 2017-06-12, under 510(k) number K171418.
Who is the listed applicant for 1417WCC_127um and1417WCC_140um?
FDA 510(k)记录将Rayence Co., Ltd.列为申请人。这本身并不能确立该设备制造商的身份。
What is the FDA product code for 1417WCC_127um and1417WCC_140um?
The FDA product code for 1417WCC_127um and1417WCC_140um is MQB.
列明Rayence 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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