Televere 数字成像系统
K号: K170975 · 2017-05-01
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器械摘要
Televere Digital Imaging System is the device name listed in this FDA 510(k) record. The listed applicant is Televere Systems. It received FDA 510(k) clearance on 2017-05-01 under 510(k) number K170975. 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 Televere Digital Imaging System?
Televere Digital Imaging System is a medical device that received FDA 510(k) clearance on 2017-05-01. The listed applicant is Televere Systems. The 510(k) number is K170975.
When did Televere Digital Imaging System receive FDA 510(k) clearance?
Televere Digital Imaging System received FDA 510(k) clearance on 2017-05-01, under 510(k) number K170975.
Who is the listed applicant for Televere Digital Imaging System?
The FDA 510(k) record lists Televere Systems as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Televere Digital Imaging System?
The FDA product code for Televere Digital Imaging System is MQB.
相关临床试验
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列明Televere Systems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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