SteriTite 容器系统 & MediTray 产品
K号: K161415 · 2017-02-10
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器械摘要
常见问题
What is the SteriTite Containers System & MediTray Products?
SteriTite Containers System & MediTray Products is a medical device that received FDA 510(k) clearance on 2017-02-10. The listed applicant is Case Medical, Inc.. The 510(k) number is K161415.
When did SteriTite Containers System & MediTray Products receive FDA 510(k) clearance?
SteriTite Containers System & MediTray Products received FDA 510(k) clearance on 2017-02-10, under 510(k) number K161415.
Who is the listed applicant for SteriTite Containers System & MediTray Products?
The FDA 510(k) record lists Case Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SteriTite Containers System & MediTray Products?
The FDA product code for SteriTite Containers System & MediTray Products is FRG.
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Case Medical, 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:FRG)
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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