FROG (玻璃过滤去除)
K号: K240355 · 2025-04-18
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器械摘要
常见问题
What is the FROG (Filter Removal of Glass)?
FROG (Filter Removal of Glass) is a medical device that received FDA 510(k) clearance on 2025-04-18. The listed applicant is Carrtech Corp. The 510(k) number is K240355.
When did FROG (Filter Removal of Glass) receive FDA 510(k) clearance?
FROG (Filter Removal of Glass) received FDA 510(k) clearance on 2025-04-18, under 510(k) number K240355.
Who is the listed applicant for FROG (Filter Removal of Glass)?
The FDA 510(k) record lists Carrtech Corp as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FROG (Filter Removal of Glass)?
The FDA product code for FROG (Filter Removal of Glass) is FMI.
相关临床试验
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相关器械(代码:FMI)
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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