Resoundant 声学驱动系统
K号: K201389 · 2020-07-10
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器械摘要
Resoundant Acoustic Driver System is the device name listed in this FDA 510(k) record. The listed applicant is Resoundant, Inc.. It received FDA 510(k) clearance on 2020-07-10 under 510(k) number K201389. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Resoundant Acoustic Driver System?
Resoundant Acoustic Driver System is a medical device that received FDA 510(k) clearance on 2020-07-10. The listed applicant is Resoundant, Inc.. The 510(k) number is K201389.
When did Resoundant Acoustic Driver System receive FDA 510(k) clearance?
Resoundant Acoustic Driver System received FDA 510(k) clearance on 2020-07-10, under 510(k) number K201389.
Who is the listed applicant for Resoundant Acoustic Driver System?
The FDA 510(k) record lists Resoundant, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Resoundant Acoustic Driver System?
The FDA product code for Resoundant Acoustic Driver System is LNH.
相关临床试验
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列明Resoundant, Inc.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：LNH）
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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