EasyMap MAP Catheter
K号: K151139 · 2016-10-18
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决定日期2016-10-18
产品代码DRF
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。
决定实质等同
器械摘要
EasyMap MAP Catheter is the device name listed in this FDA 510(k) record. The listed applicant is Medfact Engineering GmbH. It received FDA 510(k) clearance on 2016-10-18 under 510(k) number K151139. The device is classified under product code DRF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the EasyMap MAP Catheter?
EasyMap MAP Catheter is a medical device that received FDA 510(k) clearance on 2016-10-18. The listed applicant is Medfact Engineering GmbH. The 510(k) number is K151139.
When did EasyMap MAP Catheter receive FDA 510(k) clearance?
EasyMap MAP Catheter received FDA 510(k) clearance on 2016-10-18, under 510(k) number K151139.
Who is the listed applicant for EasyMap MAP Catheter?
The FDA 510(k) record lists Medfact Engineering GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EasyMap MAP Catheter?
The FDA product code for EasyMap MAP Catheter is DRF.
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。
相关器械（代码：DRF）
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。
K252794Vision-MR™诊断导管Imricor Medical Systems, Inc.K250590MAGiC Sweep™ EP Mapping CatheterStereotaxis, Inc.K250310VIKING™ 固定弯曲诊断导管Boston Scientific CorporationK240366EP•XT™ 单向可弯曲诊断导管；Dynamic Tip™ 单向可弯曲诊断导管；Dynamic XT™ 单向可弯曲诊断导管Boston Scientific CorporationK233900Nordica PV Cryo Mapping导管Synaptic Medical CorporationK233397Cosine-10TM 诊断导管Medtronic, Inc.
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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