彩虹膠質染色SE
K 號：K233885 · 2024-06-21
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器材摘要
rainbow Paste Stain SE is the device name listed in this FDA 510(k) record. The listed applicant is Genoss Co., Ltd.. It received FDA 510(k) clearance on 2024-06-21 under 510(k) number K233885. The device is classified under product code EIH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the rainbow Paste Stain SE?
rainbow Paste Stain SE is a medical device that received FDA 510(k) clearance on 2024-06-21. The listed applicant is Genoss Co., Ltd.. The 510(k) number is K233885.
When did rainbow Paste Stain SE receive FDA 510(k) clearance?
rainbow Paste Stain SE received FDA 510(k) clearance on 2024-06-21, under 510(k) number K233885.
Who is the listed applicant for rainbow Paste Stain SE?
The FDA 510(k) record lists Genoss Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for rainbow Paste Stain SE?
The FDA product code for rainbow Paste Stain SE is EIH.
相關臨床試驗
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其他以 Genoss Co., Ltd. 為申請人之記錄
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：EIH）
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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