AutoChamber
K号: K240786 · 2024-10-10
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器械摘要
AutoChamber is the device name listed in this FDA 510(k) record. The listed applicant is HeartLung Corporation. It received FDA 510(k) clearance on 2024-10-10 under 510(k) number K240786. The device is classified under product code QIH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the AutoChamber?
AutoChamber is a medical device that received FDA 510(k) clearance on 2024-10-10. The listed applicant is HeartLung Corporation. The 510(k) number is K240786.
When did AutoChamber receive FDA 510(k) clearance?
AutoChamber received FDA 510(k) clearance on 2024-10-10, under 510(k) number K240786.
Who is the listed applicant for AutoChamber?
The FDA 510(k) record lists HeartLung Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AutoChamber?
The FDA product code for AutoChamber is QIH.
相关临床试验
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列明HeartLung Corporation为申报人的其他记录
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相关器械（代码：QIH）
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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