QT Scanner 2000 型号 A
K号: K220933 · 2022-08-31
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器械摘要
QT Scanner 2000 Model A is the device name listed in this FDA 510(k) record. The listed applicant is Qt Imaging, Inc.. It received FDA 510(k) clearance on 2022-08-31 under 510(k) number K220933. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the QT Scanner 2000 Model A?
QT Scanner 2000 Model A is a medical device that received FDA 510(k) clearance on 2022-08-31. The listed applicant is Qt Imaging, Inc.. The 510(k) number is K220933.
When did QT Scanner 2000 Model A receive FDA 510(k) clearance?
QT Scanner 2000 Model A received FDA 510(k) clearance on 2022-08-31, under 510(k) number K220933.
Who is the listed applicant for QT Scanner 2000 Model A?
The FDA 510(k) record lists Qt Imaging, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for QT Scanner 2000 Model A?
The FDA product code for QT Scanner 2000 Model A is IYO.
相关临床试验
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相关器械（代码：IYO）
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。
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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