Accipiolx
K号: K182177 · 2018-10-26
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器械摘要
Accipiolx is the device name listed in this FDA 510(k) record. The listed applicant is Maxq-Al , Ltd.. It received FDA 510(k) clearance on 2018-10-26 under 510(k) number K182177. The device is classified under product code QAS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Accipiolx?
Accipiolx is a medical device that received FDA 510(k) clearance on 2018-10-26. The listed applicant is Maxq-Al , Ltd.. The 510(k) number is K182177.
When did Accipiolx receive FDA 510(k) clearance?
Accipiolx received FDA 510(k) clearance on 2018-10-26, under 510(k) number K182177.
Who is the listed applicant for Accipiolx?
The FDA 510(k) record lists Maxq-Al , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Accipiolx?
The FDA product code for Accipiolx is QAS.
相关临床试验
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列明Maxq-Al , Ltd.为申报人的其他记录
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相关器械（代码：QAS）
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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