FS Ergo
K号: K173646 · 2017-12-19
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决定日期2017-12-19
产品代码MUH
咨询委员会DE
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决定实质等同
器械摘要
FS Ergo is the device name listed in this FDA 510(k) record. The listed applicant is Palodex Group OY. It received FDA 510(k) clearance on 2017-12-19 under 510(k) number K173646. The device is classified under product code MUH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the FS Ergo?
FS Ergo is a medical device that received FDA 510(k) clearance on 2017-12-19. The listed applicant is Palodex Group OY. The 510(k) number is K173646.
When did FS Ergo receive FDA 510(k) clearance?
FS Ergo received FDA 510(k) clearance on 2017-12-19, under 510(k) number K173646.
Who is the listed applicant for FS Ergo?
The FDA 510(k) record lists Palodex Group OY as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FS Ergo?
The FDA product code for FS Ergo is MUH.
列明Palodex Group OY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：MUH）
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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