NUVISION® 超声导管；NUVISION® NAV 超声导管
K号: K241540 · 2024-06-28
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器械摘要
常见问题
What is the NUVISION™ Ultrasound Catheter; NUVISION™ NAV Ultrasound Catheter?
NUVISION™ Ultrasound Catheter; NUVISION™ NAV Ultrasound Catheter is a medical device that received FDA 510(k) clearance on 2024-06-28. The listed applicant is Biosense Webster, Inc.. The 510(k) number is K241540.
When did NUVISION™ Ultrasound Catheter; NUVISION™ NAV Ultrasound Catheter receive FDA 510(k) clearance?
NUVISION™ Ultrasound Catheter; NUVISION™ NAV Ultrasound Catheter received FDA 510(k) clearance on 2024-06-28, under 510(k) number K241540.
Who is the listed applicant for NUVISION™ Ultrasound Catheter; NUVISION™ NAV Ultrasound Catheter?
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 NUVISION™ Ultrasound Catheter; NUVISION™ NAV Ultrasound Catheter?
The FDA product code for NUVISION™ Ultrasound Catheter; NUVISION™ NAV Ultrasound Catheter is OBJ.
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。
列明Biosense Webster, Inc.为申报人的其他记录
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：OBJ）
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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