Solaris 注射器用 MR 注射器双包装
K号: K161471 · 2016-10-06
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器械摘要
常见问题
What is the MR Syringe Dual Pack for Solaris Injectors?
MR Syringe Dual Pack for Solaris Injectors is a medical device that received FDA 510(k) clearance on 2016-10-06. The listed applicant is Coeur, Inc.. The 510(k) number is K161471.
When did MR Syringe Dual Pack for Solaris Injectors receive FDA 510(k) clearance?
MR Syringe Dual Pack for Solaris Injectors received FDA 510(k) clearance on 2016-10-06, under 510(k) number K161471.
Who is the listed applicant for MR Syringe Dual Pack for Solaris Injectors?
The FDA 510(k) record lists Coeur, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MR Syringe Dual Pack for Solaris Injectors?
The FDA product code for MR Syringe Dual Pack for Solaris Injectors is DXT.
相关临床试验
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列明Coeur, 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:DXT)
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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