ArcherQA (V1.0)
K号: K231273 · 2024-01-05
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器械摘要
ArcherQA (V1.0) is the device name listed in this FDA 510(k) record. The listed applicant is Wisdom Technologies., Inc.. It received FDA 510(k) clearance on 2024-01-05 under 510(k) number K231273. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the ArcherQA (V1.0)?
ArcherQA (V1.0) is a medical device that received FDA 510(k) clearance on 2024-01-05. The listed applicant is Wisdom Technologies., Inc.. The 510(k) number is K231273.
When did ArcherQA (V1.0) receive FDA 510(k) clearance?
ArcherQA (V1.0) received FDA 510(k) clearance on 2024-01-05, under 510(k) number K231273.
Who is the listed applicant for ArcherQA (V1.0)?
The FDA 510(k) record lists Wisdom Technologies., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ArcherQA (V1.0)?
The FDA product code for ArcherQA (V1.0) is IYE.
相关临床试验
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列明Wisdom Technologies., 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：IYE）
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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