Indigo® Lightning Flash 吸引系统 – Select +™ 管道
K号: K241399 · 2024-06-10
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器械摘要
常见问题
What is the Indigo® Lightning Flash Aspiration System – Select +™ Catheter?
Indigo® Lightning Flash Aspiration System – Select +™ Catheter is a medical device that received FDA 510(k) clearance on 2024-06-10. The listed applicant is Penumbra, Inc.. The 510(k) number is K241399.
When did Indigo® Lightning Flash Aspiration System – Select +™ Catheter receive FDA 510(k) clearance?
Indigo® Lightning Flash Aspiration System – Select +™ Catheter received FDA 510(k) clearance on 2024-06-10, under 510(k) number K241399.
Who is the listed applicant for Indigo® Lightning Flash Aspiration System – Select +™ Catheter?
The FDA 510(k) record lists Penumbra, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Indigo® Lightning Flash Aspiration System – Select +™ Catheter?
The FDA product code for Indigo® Lightning Flash Aspiration System – Select +™ Catheter is QEW.
相关临床试验
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列明Penumbra, Inc.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:QEW)
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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