Tuxedo 数字牙科传感器
K号: K153710 · 2016-03-18
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器械摘要
Tuxedo Digital Dental Sensor is the device name listed in this FDA 510(k) record. The listed applicant is Led Dental, Inc.. It received FDA 510(k) clearance on 2016-03-18 under 510(k) number K153710. 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 Tuxedo Digital Dental Sensor?
Tuxedo Digital Dental Sensor is a medical device that received FDA 510(k) clearance on 2016-03-18. The listed applicant is Led Dental, Inc.. The 510(k) number is K153710.
When did Tuxedo Digital Dental Sensor receive FDA 510(k) clearance?
Tuxedo Digital Dental Sensor received FDA 510(k) clearance on 2016-03-18, under 510(k) number K153710.
Who is the listed applicant for Tuxedo Digital Dental Sensor?
The FDA 510(k) record lists Led Dental, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Tuxedo Digital Dental Sensor?
The FDA product code for Tuxedo Digital Dental Sensor 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。
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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