青光眼模块
K号: K200954 · 2020-08-03
广告
器械摘要
Glaucoma Module is the device name listed in this FDA 510(k) record. The listed applicant is Topcon Healthcare Solutions, Inc.. It received FDA 510(k) clearance on 2020-08-03 under 510(k) number K200954. The device is classified under product code NFJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Glaucoma Module?
Glaucoma Module is a medical device that received FDA 510(k) clearance on 2020-08-03. The listed applicant is Topcon Healthcare Solutions, Inc.. The 510(k) number is K200954.
When did Glaucoma Module receive FDA 510(k) clearance?
Glaucoma Module received FDA 510(k) clearance on 2020-08-03, under 510(k) number K200954.
Who is the listed applicant for Glaucoma Module?
The FDA 510(k) record lists Topcon Healthcare Solutions, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Glaucoma Module?
The FDA product code for Glaucoma Module is NFJ.
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：NFJ）
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。
广告