StimaWELL 120MTRS
K 號：K181645 · 2020-08-13
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器材摘要
StimaWELL 120MTRS is the device name listed in this FDA 510(k) record. The listed applicant is Pierenkemper GmbH. It received FDA 510(k) clearance on 2020-08-13 under 510(k) number K181645. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the StimaWELL 120MTRS?
StimaWELL 120MTRS is a medical device that received FDA 510(k) clearance on 2020-08-13. The listed applicant is Pierenkemper GmbH. The 510(k) number is K181645.
When did StimaWELL 120MTRS receive FDA 510(k) clearance?
StimaWELL 120MTRS received FDA 510(k) clearance on 2020-08-13, under 510(k) number K181645.
Who is the listed applicant for StimaWELL 120MTRS?
The FDA 510(k) record lists Pierenkemper GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for StimaWELL 120MTRS?
The FDA product code for StimaWELL 120MTRS is GZJ.
相關臨床試驗
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相關器械（代碼：GZJ）
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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