SCATTER CORRECTION FOR CXDI SERIES
K号: K153312 · 2016-06-28
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器械摘要
SCATTER CORRECTION FOR CXDI SERIES is the device name listed in this FDA 510(k) record. The listed applicant is Canon, Inc.. It received FDA 510(k) clearance on 2016-06-28 under 510(k) number K153312. 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 SCATTER CORRECTION FOR CXDI SERIES?
SCATTER CORRECTION FOR CXDI SERIES is a medical device that received FDA 510(k) clearance on 2016-06-28. The listed applicant is Canon, Inc.. The 510(k) number is K153312.
When did SCATTER CORRECTION FOR CXDI SERIES receive FDA 510(k) clearance?
SCATTER CORRECTION FOR CXDI SERIES received FDA 510(k) clearance on 2016-06-28, under 510(k) number K153312.
Who is the listed applicant for SCATTER CORRECTION FOR CXDI SERIES?
The FDA 510(k) record lists Canon, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SCATTER CORRECTION FOR CXDI SERIES?
The FDA product code for SCATTER CORRECTION FOR CXDI SERIES is MQB.
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。
列明Canon, Inc.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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