人工虹膜
PMA编号：P170039 · 2020-09-04
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决定日期2020-09-04
PMA 编号P170039
产品代码QBT
设备分类第3类
医疗专科U
咨询委员会OP
请注意，由于您没有提供具体的医疗设备监管文本，我无法进行翻译。请提供具体的文本内容，以便我能够按照您的要求进行翻译。
器械摘要
Artificial iris is the device name listed in this FDA 510(k) record. The listed applicant is Humanoptics AG. It received FDA 510(k) clearance on 2020-09-04. The device is classified under product code QBT. It was reviewed by the OP advisory panel.
常见问题
What is the Artificial iris?
Artificial iris is a medical device that received FDA 510(k) clearance on 2020-09-04. The listed applicant is Humanoptics AG.
When did Artificial iris receive FDA 510(k) clearance?
The clearance date for Artificial iris can be found in the official FDA records.
Who is the listed applicant for Artificial iris?
The FDA 510(k) record lists Humanoptics AG as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Artificial iris?
The FDA product code for Artificial iris is QBT.
相关临床试验
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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