6543Z，4386Z，4343Z，4343ZF，3543Z，3543ZF，3030Z，3025Z，3025ZF
K 號：K212105 · 2021-08-23
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器材摘要
6543Z, 4386Z, 4343Z, 4343ZF, 3543Z, 3543ZF, 3030Z, 3025Z, 3025ZF is the device name listed in this FDA 510(k) record. The listed applicant is Pzmedical Technology Co., Ltd.. It received FDA 510(k) clearance on 2021-08-23 under 510(k) number K212105. The device is classified under product code MQB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the 6543Z, 4386Z, 4343Z, 4343ZF, 3543Z, 3543ZF, 3030Z, 3025Z, 3025ZF?
6543Z, 4386Z, 4343Z, 4343ZF, 3543Z, 3543ZF, 3030Z, 3025Z, 3025ZF is a medical device that received FDA 510(k) clearance on 2021-08-23. The listed applicant is Pzmedical Technology Co., Ltd.. The 510(k) number is K212105.
When did 6543Z, 4386Z, 4343Z, 4343ZF, 3543Z, 3543ZF, 3030Z, 3025Z, 3025ZF receive FDA 510(k) clearance?
6543Z, 4386Z, 4343Z, 4343ZF, 3543Z, 3543ZF, 3030Z, 3025Z, 3025ZF received FDA 510(k) clearance on 2021-08-23, under 510(k) number K212105.
Who is the listed applicant for 6543Z, 4386Z, 4343Z, 4343ZF, 3543Z, 3543ZF, 3030Z, 3025Z, 3025ZF?
The FDA 510(k) record lists Pzmedical Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for 6543Z, 4386Z, 4343Z, 4343ZF, 3543Z, 3543ZF, 3030Z, 3025Z, 3025ZF?
The FDA product code for 6543Z, 4386Z, 4343Z, 4343ZF, 3543Z, 3543ZF, 3030Z, 3025Z, 3025ZF is MQB.
相關器械（代碼：MQB）
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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