eMotus 呼吸运动管理系统
K号: K243900 · 2025-06-27
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器械摘要
eMotus Respiratory Motion Management System is the device name listed in this FDA 510(k) record. The listed applicant is Empnia, Inc.. It received FDA 510(k) clearance on 2025-06-27 under 510(k) number K243900. The device is classified under product code LHN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the eMotus Respiratory Motion Management System?
eMotus Respiratory Motion Management System is a medical device that received FDA 510(k) clearance on 2025-06-27. The listed applicant is Empnia, Inc.. The 510(k) number is K243900.
When did eMotus Respiratory Motion Management System receive FDA 510(k) clearance?
eMotus Respiratory Motion Management System received FDA 510(k) clearance on 2025-06-27, under 510(k) number K243900.
Who is the listed applicant for eMotus Respiratory Motion Management System?
The FDA 510(k) record lists Empnia, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for eMotus Respiratory Motion Management System?
The FDA product code for eMotus Respiratory Motion Management System is LHN.
相关临床试验
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：LHN）
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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