超声波手术系统
K号: K190281 · 2019-10-31
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器械摘要
Ultrasonic Surgical System is the device name listed in this FDA 510(k) record. The listed applicant is Medisonic Technology CO. It received FDA 510(k) clearance on 2019-10-31 under 510(k) number K190281. The device is classified under product code LFL. FDA Decision: Substantially Equivalent.
常见问题
What is the Ultrasonic Surgical System?
Ultrasonic Surgical System is a medical device that received FDA 510(k) clearance on 2019-10-31. The listed applicant is Medisonic Technology CO. The 510(k) number is K190281.
When did Ultrasonic Surgical System receive FDA 510(k) clearance?
Ultrasonic Surgical System received FDA 510(k) clearance on 2019-10-31, under 510(k) number K190281.
Who is the listed applicant for Ultrasonic Surgical System?
The FDA 510(k) record lists Medisonic Technology CO as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Ultrasonic Surgical System?
The FDA product code for Ultrasonic Surgical System is LFL.
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：LFL）
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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