Forcyte 自體移植採集套件
K 號：K243407 · 2025-07-29
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器材摘要
Forcyte Autograft Harvest Kit is the device name listed in this FDA 510(k) record. The listed applicant is Forcyte Medical, LLC. It received FDA 510(k) clearance on 2025-07-29 under 510(k) number K243407. 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 Forcyte Autograft Harvest Kit?
Forcyte Autograft Harvest Kit is a medical device that received FDA 510(k) clearance on 2025-07-29. The listed applicant is Forcyte Medical, LLC. The 510(k) number is K243407.
When did Forcyte Autograft Harvest Kit receive FDA 510(k) clearance?
Forcyte Autograft Harvest Kit received FDA 510(k) clearance on 2025-07-29, under 510(k) number K243407.
Who is the listed applicant for Forcyte Autograft Harvest Kit?
The FDA 510(k) record lists Forcyte Medical, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Forcyte Autograft Harvest Kit?
The FDA product code for Forcyte Autograft Harvest Kit 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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