眼淚池可溶解淚點栓
K 號：K190210 · 2019-10-24
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器材摘要
Tear Pool Dissolvable Punctum Plugs is the device name listed in this FDA 510(k) record. The listed applicant is Alphamed, Inc.. It received FDA 510(k) clearance on 2019-10-24 under 510(k) number K190210. The device is classified under product code LZU. FDA Decision: Substantially Equivalent.
常見問題
What is the Tear Pool Dissolvable Punctum Plugs?
Tear Pool Dissolvable Punctum Plugs is a medical device that received FDA 510(k) clearance on 2019-10-24. The listed applicant is Alphamed, Inc.. The 510(k) number is K190210.
When did Tear Pool Dissolvable Punctum Plugs receive FDA 510(k) clearance?
Tear Pool Dissolvable Punctum Plugs received FDA 510(k) clearance on 2019-10-24, under 510(k) number K190210.
Who is the listed applicant for Tear Pool Dissolvable Punctum Plugs?
The FDA 510(k) record lists Alphamed, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Tear Pool Dissolvable Punctum Plugs?
The FDA product code for Tear Pool Dissolvable Punctum Plugs is LZU.
相關臨床試驗
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相關器械（代碼：LZU）
相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。
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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