Atrauman® Ag
K号: K242758 · 2024-12-09
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器械摘要
Atrauman® Ag is the device name listed in this FDA 510(k) record. The listed applicant is Hartmann USA, Inc.. It received FDA 510(k) clearance on 2024-12-09 under 510(k) number K242758. The device is classified under product code FRO. Product code FRO falls under the category of Anesthesiology, which includes devices for anesthetic delivery and patient monitoring. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.
常见问题
What is the Atrauman® Ag?
Atrauman® Ag is a medical device that received FDA 510(k) clearance on 2024-12-09. The listed applicant is Hartmann USA, Inc.. The 510(k) number is K242758.
When did Atrauman® Ag receive FDA 510(k) clearance?
Atrauman® Ag received FDA 510(k) clearance on 2024-12-09, under 510(k) number K242758.
Who is the listed applicant for Atrauman® Ag?
The FDA 510(k) record lists Hartmann USA, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Atrauman® Ag?
The FDA product code for Atrauman® Ag is FRO. This falls under the Anesthesiology category.
相关临床试验
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相关器械（代码：FRO）
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
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