Nixall抗菌解決方案™皮膚與傷口水凝膠
K 號:K243457 · 2025-05-02
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器材摘要
常見問題
What is the Nixall Antimicrobial Solutions™ Skin & Wound Hydrogel?
Nixall Antimicrobial Solutions™ Skin & Wound Hydrogel is a medical device that received FDA 510(k) clearance on 2025-05-02. The listed applicant is Seriously Clean, Ltd.. The 510(k) number is K243457.
When did Nixall Antimicrobial Solutions™ Skin & Wound Hydrogel receive FDA 510(k) clearance?
Nixall Antimicrobial Solutions™ Skin & Wound Hydrogel received FDA 510(k) clearance on 2025-05-02, under 510(k) number K243457.
Who is the listed applicant for Nixall Antimicrobial Solutions™ Skin & Wound Hydrogel?
The FDA 510(k) record lists Seriously Clean, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Nixall Antimicrobial Solutions™ Skin & Wound Hydrogel?
The FDA product code for Nixall Antimicrobial Solutions™ Skin & Wound Hydrogel is FRO. This falls under the Anesthesiology category.
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相關器械(代碼:FRO)
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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