Prelude IDeal 9F 润滑鞘引入器
K号: K212152 · 2022-01-07
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器械摘要
常见问题
What is the Prelude IDeal 9F Hydrophilic Sheath Introducer?
Prelude IDeal 9F Hydrophilic Sheath Introducer is a medical device that received FDA 510(k) clearance on 2022-01-07. The listed applicant is Merit Medical Systems. The 510(k) number is K212152.
When did Prelude IDeal 9F Hydrophilic Sheath Introducer receive FDA 510(k) clearance?
Prelude IDeal 9F Hydrophilic Sheath Introducer received FDA 510(k) clearance on 2022-01-07, under 510(k) number K212152.
Who is the listed applicant for Prelude IDeal 9F Hydrophilic Sheath Introducer?
The FDA 510(k) record lists Merit Medical Systems as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Prelude IDeal 9F Hydrophilic Sheath Introducer?
The FDA product code for Prelude IDeal 9F Hydrophilic Sheath Introducer 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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