角膜植入物，屈光
PMA编号：P120023 · 2017-07-18
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申请人Corneagen
决定日期2017-07-18
PMA 编号P120023
产品代码LQE
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
Implant, corneal, refractive is the device name listed in this FDA 510(k) record. The listed applicant is Corneagen. It received FDA 510(k) clearance on 2017-07-18. The device is classified under product code LQE. It was reviewed by the OP advisory panel.
常见问题
What is the Implant, corneal, refractive?
Implant, corneal, refractive is a medical device that received FDA 510(k) clearance on 2017-07-18. The listed applicant is Corneagen.
When did Implant, corneal, refractive receive FDA 510(k) clearance?
The clearance date for Implant, corneal, refractive can be found in the official FDA records.
Who is the listed applicant for Implant, corneal, refractive?
The FDA 510(k) record lists Corneagen as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Implant, corneal, refractive?
The FDA product code for Implant, corneal, refractive is LQE.
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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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