R2P 目的地细引导套管
K号: K171491 · 2017-10-05
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器械摘要
常见问题
What is the R2P Destination Slender Guiding Sheath?
R2P Destination Slender Guiding Sheath is a medical device that received FDA 510(k) clearance on 2017-10-05. The listed applicant is Terumo Medical Corporation. The 510(k) number is K171491.
When did R2P Destination Slender Guiding Sheath receive FDA 510(k) clearance?
R2P Destination Slender Guiding Sheath received FDA 510(k) clearance on 2017-10-05, under 510(k) number K171491.
Who is the listed applicant for R2P Destination Slender Guiding Sheath?
The FDA 510(k) record lists Terumo Medical Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for R2P Destination Slender Guiding Sheath?
The FDA product code for R2P Destination Slender Guiding 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Terumo Medical Corporation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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