CanGaroo RM 抗菌信封
K 號：K233991 · 2024-06-14
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器材摘要
CanGaroo RM Antibacterial Envelope is the device name listed in this FDA 510(k) record. The listed applicant is Elutia, Inc.. It received FDA 510(k) clearance on 2024-06-14 under 510(k) number K233991. The device is classified under product code FTM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the CanGaroo RM Antibacterial Envelope?
CanGaroo RM Antibacterial Envelope is a medical device that received FDA 510(k) clearance on 2024-06-14. The listed applicant is Elutia, Inc.. The 510(k) number is K233991.
When did CanGaroo RM Antibacterial Envelope receive FDA 510(k) clearance?
CanGaroo RM Antibacterial Envelope received FDA 510(k) clearance on 2024-06-14, under 510(k) number K233991.
Who is the listed applicant for CanGaroo RM Antibacterial Envelope?
The FDA 510(k) record lists Elutia, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CanGaroo RM Antibacterial Envelope?
The FDA product code for CanGaroo RM Antibacterial Envelope is FTM.
相關臨床試驗
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。
相關器械（代碼：FTM）
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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