多焦点人工晶状体
PMA编号：P060011 · 2026-09-24
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决定日期2026-09-24
PMA 编号P060011
产品代码MFK
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
器械摘要
Lens, multifocal intraocular is the device name listed in this FDA 510(k) record. The listed applicant is Rayner Intraocular Lenses , Ltd.. It received FDA 510(k) clearance on 2026-09-24. The device is classified under product code MFK. It was reviewed by the OP advisory panel.
常见问题
What is the Lens, multifocal intraocular?
Lens, multifocal intraocular is a medical device that received FDA 510(k) clearance on 2026-09-24. The listed applicant is Rayner Intraocular Lenses , Ltd..
When did Lens, multifocal intraocular receive FDA 510(k) clearance?
The clearance date for Lens, multifocal intraocular can be found in the official FDA records.
Who is the listed applicant for Lens, multifocal intraocular?
The FDA 510(k) record lists Rayner Intraocular Lenses , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Lens, multifocal intraocular?
The FDA product code for Lens, multifocal intraocular is MFK.
相关临床试验
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官方来源
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