Prelude
K号: K180308 · 2018-03-27
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器械摘要
Prelude is the device name listed in this FDA 510(k) record. The listed applicant is Medcom GmbH. It received FDA 510(k) clearance on 2018-03-27 under 510(k) number K180308. The device is classified under product code MUJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Prelude?
Prelude is a medical device that received FDA 510(k) clearance on 2018-03-27. The listed applicant is Medcom GmbH. The 510(k) number is K180308.
When did Prelude receive FDA 510(k) clearance?
Prelude received FDA 510(k) clearance on 2018-03-27, under 510(k) number K180308.
Who is the listed applicant for Prelude?
The FDA 510(k) record lists Medcom GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Prelude?
The FDA product code for Prelude is MUJ.
相关临床试验
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列明Medcom GmbH为申报人的其他记录
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相关器械（代码：MUJ）
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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