Lumina-PTFE 鈦金屬
K 號：K221851 · 2023-12-08
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器材摘要
Lumina-PTFE Titanium is the device name listed in this FDA 510(k) record. The listed applicant is Criteria Industria E Comercio DE Produtos Medicinais. It received FDA 510(k) clearance on 2023-12-08 under 510(k) number K221851. The device is classified under product code NPK. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Lumina-PTFE Titanium?
Lumina-PTFE Titanium is a medical device that received FDA 510(k) clearance on 2023-12-08. The listed applicant is Criteria Industria E Comercio DE Produtos Medicinais. The 510(k) number is K221851.
When did Lumina-PTFE Titanium receive FDA 510(k) clearance?
Lumina-PTFE Titanium received FDA 510(k) clearance on 2023-12-08, under 510(k) number K221851.
Who is the listed applicant for Lumina-PTFE Titanium?
The FDA 510(k) record lists Criteria Industria E Comercio DE Produtos Medicinais as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Lumina-PTFE Titanium?
The FDA product code for Lumina-PTFE Titanium is NPK.
相關臨床試驗
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相關器械（代碼：NPK）
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。
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官方來源
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