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PMA 核准號：P240038 · 2026-09-25
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決定日期2026-09-25
PMA 編號P240038
產品代碼HQL
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
intraocular lens is the device name listed in this FDA 510(k) record. The listed applicant is Beaver Visitec International, Inc.. It received FDA 510(k) clearance on 2026-09-25. The device is classified under product code HQL. It was reviewed by the OP advisory panel.
常見問題
What is the intraocular lens?
intraocular lens is a medical device that received FDA 510(k) clearance on 2026-09-25. The listed applicant is Beaver Visitec International, Inc..
When did intraocular lens receive FDA 510(k) clearance?
The clearance date for intraocular lens can be found in the official FDA records.
Who is the listed applicant for intraocular lens?
The FDA 510(k) record lists Beaver Visitec International, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for intraocular lens?
The FDA product code for intraocular lens is HQL.
相關臨床試驗
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官方來源
在 FDA 資料庫中查看 →資料來源為 FDA Open API。如需最新且權威的資訊，請始終參閱官方記錄。
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