系统，血管内移植物，动静脉（AV）透析通路狭窄治疗
PMA编号：P060002 · 2018-10-11
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决定日期2018-10-11
PMA 编号P060002
产品代码PFV
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：
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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]
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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
System, endovascular graft, arteriovenous (AV) dialysis access circuit stenosis treatment is the device name listed in this FDA 510(k) record. The listed applicant is Bard Peripheral Vascular. It received FDA 510(k) clearance on 2018-10-11. The device is classified under product code PFV. It was reviewed by the CV advisory panel.
常见问题
What is the System, endovascular graft, arteriovenous (AV) dialysis access circuit stenosis treatment?
System, endovascular graft, arteriovenous (AV) dialysis access circuit stenosis treatment is a medical device that received FDA 510(k) clearance on 2018-10-11. The listed applicant is Bard Peripheral Vascular.
When did System, endovascular graft, arteriovenous (AV) dialysis access circuit stenosis treatment receive FDA 510(k) clearance?
The clearance date for System, endovascular graft, arteriovenous (AV) dialysis access circuit stenosis treatment can be found in the official FDA records.
Who is the listed applicant for System, endovascular graft, arteriovenous (AV) dialysis access circuit stenosis treatment?
The FDA 510(k) record lists Bard Peripheral Vascular as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for System, endovascular graft, arteriovenous (AV) dialysis access circuit stenosis treatment?
The FDA product code for System, endovascular graft, arteriovenous (AV) dialysis access circuit stenosis treatment is PFV.
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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