TDS標準溶液
K 號：K191496 · 2019-08-05
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器材摘要
TDS Standard Solution is the device name listed in this FDA 510(k) record. The listed applicant is Mesa Laboratories, Inc.. It received FDA 510(k) clearance on 2019-08-05 under 510(k) number K191496. The device is classified under product code FKH. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the TDS Standard Solution?
TDS Standard Solution is a medical device that received FDA 510(k) clearance on 2019-08-05. The listed applicant is Mesa Laboratories, Inc.. The 510(k) number is K191496.
When did TDS Standard Solution receive FDA 510(k) clearance?
TDS Standard Solution received FDA 510(k) clearance on 2019-08-05, under 510(k) number K191496.
Who is the listed applicant for TDS Standard Solution?
The FDA 510(k) record lists Mesa Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TDS Standard Solution?
The FDA product code for TDS Standard Solution is FKH.
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其他以 Mesa Laboratories, Inc. 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。
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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