AVIEW RT ACS
K号: K220408 · 2022-11-10
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器械摘要
AVIEW RT ACS is the device name listed in this FDA 510(k) record. The listed applicant is Coreline Soft Co., Ltd.. It received FDA 510(k) clearance on 2022-11-10 under 510(k) number K220408. The device is classified under product code QKB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the AVIEW RT ACS?
AVIEW RT ACS is a medical device that received FDA 510(k) clearance on 2022-11-10. The listed applicant is Coreline Soft Co., Ltd.. The 510(k) number is K220408.
When did AVIEW RT ACS receive FDA 510(k) clearance?
AVIEW RT ACS received FDA 510(k) clearance on 2022-11-10, under 510(k) number K220408.
Who is the listed applicant for AVIEW RT ACS?
The FDA 510(k) record lists Coreline Soft Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AVIEW RT ACS?
The FDA product code for AVIEW RT ACS is QKB.
相关临床试验
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列明Coreline Soft Co., 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：QKB）
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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