Compremium隔室压缩性监测系统（CPM#1）
K号: K223509 · 2023-04-14
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器械摘要
Compremium Compartment Compressibility Monitoring System (CPM#1) is the device name listed in this FDA 510(k) record. The listed applicant is Compremium AG. It received FDA 510(k) clearance on 2023-04-14 under 510(k) number K223509. The device is classified under product code LXC. FDA Decision: Substantially Equivalent.
常见问题
What is the Compremium Compartment Compressibility Monitoring System (CPM#1)?
Compremium Compartment Compressibility Monitoring System (CPM#1) is a medical device that received FDA 510(k) clearance on 2023-04-14. The listed applicant is Compremium AG. The 510(k) number is K223509.
When did Compremium Compartment Compressibility Monitoring System (CPM#1) receive FDA 510(k) clearance?
Compremium Compartment Compressibility Monitoring System (CPM#1) received FDA 510(k) clearance on 2023-04-14, under 510(k) number K223509.
Who is the listed applicant for Compremium Compartment Compressibility Monitoring System (CPM#1)?
The FDA 510(k) record lists Compremium AG as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Compremium Compartment Compressibility Monitoring System (CPM#1)?
The FDA product code for Compremium Compartment Compressibility Monitoring System (CPM#1) is LXC.
相关临床试验
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相关器械（代码：LXC）
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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