Avid CT2
K号: K202490 · 2020-11-16
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决定日期2020-11-16
产品代码IPF
咨询委员会PM
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决定实质等同
器械摘要
Avid CT2 is the device name listed in this FDA 510(k) record. The listed applicant is Vision Quest Industries Inc./Dba VQ Orthocare. It received FDA 510(k) clearance on 2020-11-16 under 510(k) number K202490. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Avid CT2?
Avid CT2 is a medical device that received FDA 510(k) clearance on 2020-11-16. The listed applicant is Vision Quest Industries Inc./Dba VQ Orthocare. The 510(k) number is K202490.
When did Avid CT2 receive FDA 510(k) clearance?
Avid CT2 received FDA 510(k) clearance on 2020-11-16, under 510(k) number K202490.
Who is the listed applicant for Avid CT2?
The FDA 510(k) record lists Vision Quest Industries Inc./Dba VQ Orthocare as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Avid CT2?
The FDA product code for Avid CT2 is IPF.
列明Vision Quest Industries Inc./Dba VQ Orthocare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：IPF）
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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