眼内透镜
PMA编号：P100016 · 2026-08-17
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决定日期2026-08-17
PMA 编号P100016
产品代码HQL
设备分类第3类
医疗专科O
法规编号21 CFR 8
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
intraocular lens is the device name listed in this FDA 510(k) record. The listed applicant is Carl Zeiss Meditec Production, LLC. It received FDA 510(k) clearance on 2026-08-17. The device is classified under product code HQL. It was reviewed by the OP advisory panel.
常见问题
What is the intraocular lens?
intraocular lens is a medical device that received FDA 510(k) clearance on 2026-08-17. The listed applicant is Carl Zeiss Meditec Production, LLC.
When did intraocular lens receive FDA 510(k) clearance?
The clearance date for intraocular lens can be found in the official FDA records.
眼内透镜的申请人名单是谁？
The FDA 510(k) record lists Carl Zeiss Meditec Production, LLC as the applicant. This does not by itself establish the device manufacturer.
FDA产品代码是什么，用于人工晶状体？
FDA产品代码对于人工晶状体是HQL。
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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