MTA2.2 材質
K 號：K161239 · 2016-09-01
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器材摘要
MTA2.2 MATERIAL is the device name listed in this FDA 510(k) record. The listed applicant is Avalon Biomed, Inc.. It received FDA 510(k) clearance on 2016-09-01 under 510(k) number K161239. The device is classified under product code KIF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the MTA2.2 MATERIAL?
MTA2.2 MATERIAL is a medical device that received FDA 510(k) clearance on 2016-09-01. The listed applicant is Avalon Biomed, Inc.. The 510(k) number is K161239.
When did MTA2.2 MATERIAL receive FDA 510(k) clearance?
MTA2.2 MATERIAL received FDA 510(k) clearance on 2016-09-01, under 510(k) number K161239.
Who is the listed applicant for MTA2.2 MATERIAL?
The FDA 510(k) record lists Avalon Biomed, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MTA2.2 MATERIAL?
The FDA product code for MTA2.2 MATERIAL is KIF.
相關臨床試驗
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相關器械（代碼：KIF）
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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