VedDilator ^TM（三阶段球囊扩张导管）
K号: K232245 · 2024-02-15
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器械摘要
常见问题
What is the VedDilator ^TM (3-Stage Balloon Dilation Catheter)?
VedDilator ^TM (3-Stage Balloon Dilation Catheter) is a medical device that received FDA 510(k) clearance on 2024-02-15. The listed applicant is Jiangsu Vedkang Medical Science and Technology Co., Ltd.. The 510(k) number is K232245.
When did VedDilator ^TM (3-Stage Balloon Dilation Catheter) receive FDA 510(k) clearance?
VedDilator ^TM (3-Stage Balloon Dilation Catheter) received FDA 510(k) clearance on 2024-02-15, under 510(k) number K232245.
Who is the listed applicant for VedDilator ^TM (3-Stage Balloon Dilation Catheter)?
The FDA 510(k) record lists Jiangsu Vedkang Medical Science and Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VedDilator ^TM (3-Stage Balloon Dilation Catheter)?
The FDA product code for VedDilator ^TM (3-Stage Balloon Dilation Catheter) is FGE.
相关临床试验
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列明Jiangsu Vedkang Medical Science and Technology Co., Ltd.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：FGE）
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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