FREEPRINT® 支具大师
K号: K232448 · 2023-10-12
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器械摘要
FREEPRINT® splintmaster is the device name listed in this FDA 510(k) record. The listed applicant is Detax GmbH. It received FDA 510(k) clearance on 2023-10-12 under 510(k) number K232448. The device is classified under product code MQC. FDA Decision: Substantially Equivalent.
常见问题
What is the FREEPRINT® splintmaster?
FREEPRINT® splintmaster is a medical device that received FDA 510(k) clearance on 2023-10-12. The listed applicant is Detax GmbH. The 510(k) number is K232448.
When did FREEPRINT® splintmaster receive FDA 510(k) clearance?
FREEPRINT® splintmaster received FDA 510(k) clearance on 2023-10-12, under 510(k) number K232448.
Who is the listed applicant for FREEPRINT® splintmaster?
The FDA 510(k) record lists Detax GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FREEPRINT® splintmaster?
The FDA product code for FREEPRINT® splintmaster is MQC.
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。
列明Detax GmbH为申报人的其他记录
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：MQC）
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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