SureFlex HD 可弯曲鞘，VersaCross HD 可弯曲鞘
K号: K231227 · 2023-12-20
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器械摘要
常见问题
What is the SureFlex HD Steerable Sheath, VersaCross HD Steerable Sheath?
SureFlex HD Steerable Sheath, VersaCross HD Steerable Sheath is a medical device that received FDA 510(k) clearance on 2023-12-20. The listed applicant is Baylis Medical Company, Inc.. The 510(k) number is K231227.
When did SureFlex HD Steerable Sheath, VersaCross HD Steerable Sheath receive FDA 510(k) clearance?
SureFlex HD Steerable Sheath, VersaCross HD Steerable Sheath received FDA 510(k) clearance on 2023-12-20, under 510(k) number K231227.
Who is the listed applicant for SureFlex HD Steerable Sheath, VersaCross HD Steerable Sheath?
The FDA 510(k) record lists Baylis Medical Company, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SureFlex HD Steerable Sheath, VersaCross HD Steerable Sheath?
The FDA product code for SureFlex HD Steerable Sheath, VersaCross HD Steerable Sheath is DYB.
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Baylis Medical Company, 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：DYB）
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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