髂骨覆盖支架，动脉
PMA编号：P160024 · 2025-09-29
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决定日期2025-09-29
PMA 编号P160024
产品代码PRL
设备分类第3类
医疗专科U
咨询委员会CV
请注意，由于原文未提供具体内容，以下是一个示例翻译：
---
产品名称：[产品名称]
公司名称：[公司名称]
FDA批准号：[FDA批准号]
510(k)申请号：[510(k)申请号]
PMA申请号：[PMA申请号]
临床试验注册号：[NCT]
PubMed ID：[PMID]
产品标识符：[标识符]
产品URL：[URL]
---
请将上述示例中的[产品名称]、[公司名称]、[FDA批准号]等占位符替换为实际内容。
器械摘要
Iliac covered stent, arterial is the device name listed in this FDA 510(k) record. The listed applicant is Bard Peripheral Vascular, Inc.. It received FDA 510(k) clearance on 2025-09-29. The device is classified under product code PRL. It was reviewed by the CV advisory panel.
常见问题
What is the Iliac covered stent, arterial?
Iliac covered stent, arterial is a medical device that received FDA 510(k) clearance on 2025-09-29. The listed applicant is Bard Peripheral Vascular, Inc..
When did Iliac covered stent, arterial receive FDA 510(k) clearance?
The clearance date for Iliac covered stent, arterial can be found in the official FDA records.
Who is the listed applicant for Iliac covered stent, arterial?
FDA 510(k)记录将Bard Peripheral Vascular, Inc.列为申请人。这本身并不能确立该设备制造商的身份。
What is the FDA product code for Iliac covered stent, arterial?
The FDA product code for Iliac covered stent, arterial is PRL.
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。
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