Lens, multifocal intraocular
PMA 核准號：P060011 · 2026-09-24
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決定日期2026-09-24
PMA 編號P060011
產品代碼MFK
器械分類3 類
醫療專科O
法規編號21 CFR 8
諮詢委員會OP
器材摘要
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.
常見問題
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.
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官方來源
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