EchoSolv AS
K号: K241245 · 2024-10-04
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器械摘要
EchoSolv AS is the device name listed in this FDA 510(k) record. The listed applicant is Echo IQ, Ltd.. It received FDA 510(k) clearance on 2024-10-04 under 510(k) number K241245. The device is classified under product code POK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the EchoSolv AS?
EchoSolv AS is a medical device that received FDA 510(k) clearance on 2024-10-04. The listed applicant is Echo IQ, Ltd.. The 510(k) number is K241245.
When did EchoSolv AS receive FDA 510(k) clearance?
EchoSolv AS received FDA 510(k) clearance on 2024-10-04, under 510(k) number K241245.
Who is the listed applicant for EchoSolv AS?
The FDA 510(k) record lists Echo IQ, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EchoSolv AS?
The FDA product code for EchoSolv AS is POK.
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相关器械（代码：POK）
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
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