ProCell外科海绵-血液回收單位
K 號：K193361 · 2020-06-01
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器材摘要
ProCell Surgical Sponge-Blood Recovery Unit is the device name listed in this FDA 510(k) record. The listed applicant is Procell Surgical, Inc.. It received FDA 510(k) clearance on 2020-06-01 under 510(k) number K193361. The device is classified under product code CAC. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the ProCell Surgical Sponge-Blood Recovery Unit?
ProCell Surgical Sponge-Blood Recovery Unit is a medical device that received FDA 510(k) clearance on 2020-06-01. The listed applicant is Procell Surgical, Inc.. The 510(k) number is K193361.
When did ProCell Surgical Sponge-Blood Recovery Unit receive FDA 510(k) clearance?
ProCell Surgical Sponge-Blood Recovery Unit received FDA 510(k) clearance on 2020-06-01, under 510(k) number K193361.
Who is the listed applicant for ProCell Surgical Sponge-Blood Recovery Unit?
The FDA 510(k) record lists Procell Surgical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ProCell Surgical Sponge-Blood Recovery Unit?
The FDA product code for ProCell Surgical Sponge-Blood Recovery Unit is CAC.
相關臨床試驗
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相關器械（代碼：CAC）
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
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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