Resitu Slider 09 (RESL09)
K 號：K252183 · 2025-09-24
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器材摘要
Resitu Slider 09 (RESL09) is the device name listed in this FDA 510(k) record. The listed applicant is Resitu Medical AB. It received FDA 510(k) clearance on 2025-09-24 under 510(k) number K252183. The device is classified under product code KNW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Resitu Slider 09 (RESL09)?
Resitu Slider 09 (RESL09) is a medical device that received FDA 510(k) clearance on 2025-09-24. The listed applicant is Resitu Medical AB. The 510(k) number is K252183.
When did Resitu Slider 09 (RESL09) receive FDA 510(k) clearance?
Resitu Slider 09 (RESL09) received FDA 510(k) clearance on 2025-09-24, under 510(k) number K252183.
Who is the listed applicant for Resitu Slider 09 (RESL09)?
The FDA 510(k) record lists Resitu Medical AB as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Resitu Slider 09 (RESL09)?
The FDA product code for Resitu Slider 09 (RESL09) is KNW.
相關臨床試驗
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相關器械（代碼：KNW）
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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