降低眼内压植入物
PMA编号：P150037 · 2020-04-09
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决定日期2020-04-09
PMA 编号P150037
产品代码OGO
设备分类第3类
医疗专科U
咨询委员会OP
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器械摘要
Intraocular pressure lowering implant is the device name listed in this FDA 510(k) record. The listed applicant is Alcon Research, Ltd.. It received FDA 510(k) clearance on 2020-04-09. The device is classified under product code OGO. It was reviewed by the OP advisory panel.
常见问题
What is the Intraocular pressure lowering implant?
Intraocular pressure lowering implant is a medical device that received FDA 510(k) clearance on 2020-04-09. The listed applicant is Alcon Research, Ltd..
When did Intraocular pressure lowering implant receive FDA 510(k) clearance?
The clearance date for Intraocular pressure lowering implant can be found in the official FDA records.
Who is the listed applicant for Intraocular pressure lowering implant?
The FDA 510(k) record lists Alcon Research, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Intraocular pressure lowering implant?
The FDA product code for Intraocular pressure lowering implant is OGO.
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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