眼内透镜
PMA编号：P060022 · 2026-09-03
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决定日期2026-09-03
PMA 编号P060022
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 Bausch & Lomb, Inc.. It received FDA 510(k) clearance on 2026-09-03. 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 2026-09-03. The listed applicant is Bausch & Lomb, Inc..
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 Bausch & Lomb, Inc. 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
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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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