Lim Precision Steerable TS,Steerable Sheath,Dilator
K号: K202226 · 2020-12-15
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器械摘要
常见问题
What is the Lim Precision Steerable TS, Steerable Sheath, Dilator?
Lim Precision Steerable TS, Steerable Sheath, Dilator is a medical device that received FDA 510(k) clearance on 2020-12-15. The listed applicant is Keystone Heart, Ltd.. The 510(k) number is K202226.
When did Lim Precision Steerable TS, Steerable Sheath, Dilator receive FDA 510(k) clearance?
Lim Precision Steerable TS, Steerable Sheath, Dilator received FDA 510(k) clearance on 2020-12-15, under 510(k) number K202226.
Who is the listed applicant for Lim Precision Steerable TS, Steerable Sheath, Dilator?
The FDA 510(k) record lists Keystone Heart, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Lim Precision Steerable TS, Steerable Sheath, Dilator?
The FDA product code for Lim Precision Steerable TS, Steerable Sheath, Dilator 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。
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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