Fixtemp® C&B 4:1
K号: K241226 · 2024-05-31
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决定日期2024-05-31
产品代码EBG
咨询委员会DE
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决定实质等同
器械摘要
Fixtemp® C&B 4:1 is the device name listed in this FDA 510(k) record. The listed applicant is Dreve Denatmid GmbH. It received FDA 510(k) clearance on 2024-05-31 under 510(k) number K241226. The device is classified under product code EBG. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Fixtemp® C&B 4:1?
Fixtemp® C&B 4:1 is a medical device that received FDA 510(k) clearance on 2024-05-31. The listed applicant is Dreve Denatmid GmbH. The 510(k) number is K241226.
When did Fixtemp® C&B 4:1 receive FDA 510(k) clearance?
Fixtemp® C&B 4:1 received FDA 510(k) clearance on 2024-05-31, under 510(k) number K241226.
Who is the listed applicant for Fixtemp® C&B 4:1?
The FDA 510(k) record lists Dreve Denatmid GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Fixtemp® C&B 4:1?
The FDA product code for Fixtemp® C&B 4:1 is EBG.
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相关器械（代码：EBG）
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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