超扫描650
K号: K161919 · 2017-04-05
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器械摘要
UltraScan 650 is the device name listed in this FDA 510(k) record. The listed applicant is Cyberlogic, Inc.. It received FDA 510(k) clearance on 2017-04-05 under 510(k) number K161919. The device is classified under product code MUA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the UltraScan 650?
UltraScan 650 is a medical device that received FDA 510(k) clearance on 2017-04-05. The listed applicant is Cyberlogic, Inc.. The 510(k) number is K161919.
When did UltraScan 650 receive FDA 510(k) clearance?
UltraScan 650 received FDA 510(k) clearance on 2017-04-05, under 510(k) number K161919.
Who is the listed applicant for UltraScan 650?
The FDA 510(k) record lists Cyberlogic, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for UltraScan 650?
The FDA product code for UltraScan 650 is MUA.
相关临床试验
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相关器械（代码：MUA）
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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