WEGO-PGLA 快速
K号: K183001 · 2019-01-28
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器械摘要
常见问题
What is the WEGO-PGLA RAPID?
WEGO-PGLA RAPID is a medical device that received FDA 510(k) clearance on 2019-01-28. The listed applicant is Foosin Medical Supplies Inc., Ltd.. The 510(k) number is K183001.
When did WEGO-PGLA RAPID receive FDA 510(k) clearance?
WEGO-PGLA RAPID received FDA 510(k) clearance on 2019-01-28, under 510(k) number K183001.
Who is the listed applicant for WEGO-PGLA RAPID?
The FDA 510(k) record lists Foosin Medical Supplies Inc., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for WEGO-PGLA RAPID?
The FDA product code for WEGO-PGLA RAPID is GAM.
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Foosin Medical Supplies Inc., Ltd.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:GAM)
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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