AS-10
K号: K200887 · 2020-04-15
广告
器械摘要
AS-10 is the device name listed in this FDA 510(k) record. The listed applicant is Canon, Inc.. It received FDA 510(k) clearance on 2020-04-15 under 510(k) number K200887. The device is classified under product code OWB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the AS-10?
AS-10 is a medical device that received FDA 510(k) clearance on 2020-04-15. The listed applicant is Canon, Inc.. The 510(k) number is K200887.
When did AS-10 receive FDA 510(k) clearance?
AS-10 received FDA 510(k) clearance on 2020-04-15, under 510(k) number K200887.
Who is the listed applicant for AS-10?
The FDA 510(k) record lists Canon, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AS-10?
The FDA product code for AS-10 is OWB.
列明Canon, 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：OWB）
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