电极记录导管或电极探针，电极记录
PMA编号：P990025 · 2025-02-25
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决定日期2025-02-25
PMA 编号P990025
产品代码DRF
设备分类第2类
医疗专科C
法规编号21 CFR 8
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]
---
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
CATHETER, ELECTRODE RECORDING, OR PROBE, ELECTRODE RECORDING is the device name listed in this FDA 510(k) record. The listed applicant is Biosense Webster, Inc.. It received FDA 510(k) clearance on 2025-02-25. The device is classified under product code DRF. It was reviewed by the CV advisory panel.
常见问题
What is the CATHETER, ELECTRODE RECORDING, OR PROBE, ELECTRODE RECORDING?
CATHETER, ELECTRODE RECORDING, OR PROBE, ELECTRODE RECORDING is a medical device that received FDA 510(k) clearance on 2025-02-25. The listed applicant is Biosense Webster, Inc..
When did CATHETER, ELECTRODE RECORDING, OR PROBE, ELECTRODE RECORDING receive FDA 510(k) clearance?
The clearance date for CATHETER, ELECTRODE RECORDING, OR PROBE, ELECTRODE RECORDING can be found in the official FDA records.
Who is the listed applicant for CATHETER, ELECTRODE RECORDING, OR PROBE, ELECTRODE RECORDING?
The FDA 510(k) record lists Biosense Webster, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CATHETER, ELECTRODE RECORDING, OR PROBE, ELECTRODE RECORDING?
The FDA product code for CATHETER, ELECTRODE RECORDING, OR PROBE, ELECTRODE RECORDING 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。
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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