Avantik VTM
K号: K233449 · 2024-07-15
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器械摘要
常见问题
What is the Avantik VTM?
Avantik VTM is a medical device that received FDA 510(k) clearance on 2024-07-15. The listed applicant is Hanchang Medic Co., Ltd. (Han Chang Medic). The 510(k) number is K233449.
When did Avantik VTM receive FDA 510(k) clearance?
Avantik VTM received FDA 510(k) clearance on 2024-07-15, under 510(k) number K233449.
Who is the listed applicant for Avantik VTM?
The FDA 510(k) record lists Hanchang Medic Co., Ltd. (Han Chang Medic) as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Avantik VTM?
The FDA product code for Avantik VTM is JSM.
相关临床试验
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相关器械(代码:JSM)
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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