神经血管液体栓塞剂
PMA编号：P250009 · 2026-09-09
广告
决定日期2026-09-09
PMA 编号P250009
产品代码SGU
设备分类第3类
医疗专科U
咨询委员会NE
请注意，您提供的文本“NE”不足以进行翻译，因为它不是一个完整的句子或描述。请提供完整的医疗设备监管文本，以便我能够进行准确的翻译。
器械摘要
Neurovascular Liquid Embolic Agent is the device name listed in this FDA 510(k) record. The listed applicant is Balt USA, LLC. It received FDA 510(k) clearance on 2026-09-09. The device is classified under product code SGU. It was reviewed by the NE advisory panel.
常见问题
What is the Neurovascular Liquid Embolic Agent?
Neurovascular Liquid Embolic Agent is a medical device that received FDA 510(k) clearance on 2026-09-09. The listed applicant is Balt USA, LLC.
When did Neurovascular Liquid Embolic Agent receive FDA 510(k) clearance?
The clearance date for Neurovascular Liquid Embolic Agent can be found in the official FDA records.
神经血管液体栓塞剂的列名申请人是谁？
The FDA 510(k) record lists Balt USA, LLC as the applicant. This does not by itself establish the device manufacturer.
什么是神经血管液体栓塞剂的FDA产品代码？
FDA产品代码为神经血管液体栓塞剂的代码是SGU。
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。
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。
广告