AXUS ES-5 電針設備
K 號：K200636 · 2021-02-03
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器材摘要
AXUS ES-5 Electro-Acupuncture Device is the device name listed in this FDA 510(k) record. The listed applicant is Lhasa Oms, Inc.. It received FDA 510(k) clearance on 2021-02-03 under 510(k) number K200636. The device is classified under product code BWK. FDA Decision: Substantially Equivalent.
常見問題
What is the AXUS ES-5 Electro-Acupuncture Device?
AXUS ES-5 Electro-Acupuncture Device is a medical device that received FDA 510(k) clearance on 2021-02-03. The listed applicant is Lhasa Oms, Inc.. The 510(k) number is K200636.
When did AXUS ES-5 Electro-Acupuncture Device receive FDA 510(k) clearance?
AXUS ES-5 Electro-Acupuncture Device received FDA 510(k) clearance on 2021-02-03, under 510(k) number K200636.
Who is the listed applicant for AXUS ES-5 Electro-Acupuncture Device?
The FDA 510(k) record lists Lhasa Oms, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AXUS ES-5 Electro-Acupuncture Device?
The FDA product code for AXUS ES-5 Electro-Acupuncture Device is BWK.
相關臨床試驗
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相關器械（代碼：BWK）
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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