LifePath 遠端病人監控平台
K 號：K211822 · 2022-02-03
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器材摘要
LifePath Remote Patient Monitoring Platform is the device name listed in this FDA 510(k) record. The listed applicant is Elastic Care Incorporated. It received FDA 510(k) clearance on 2022-02-03 under 510(k) number K211822. The device is classified under product code DRG. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the LifePath Remote Patient Monitoring Platform?
LifePath Remote Patient Monitoring Platform is a medical device that received FDA 510(k) clearance on 2022-02-03. The listed applicant is Elastic Care Incorporated. The 510(k) number is K211822.
When did LifePath Remote Patient Monitoring Platform receive FDA 510(k) clearance?
LifePath Remote Patient Monitoring Platform received FDA 510(k) clearance on 2022-02-03, under 510(k) number K211822.
Who is the listed applicant for LifePath Remote Patient Monitoring Platform?
The FDA 510(k) record lists Elastic Care Incorporated as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LifePath Remote Patient Monitoring Platform?
The FDA product code for LifePath Remote Patient Monitoring Platform is DRG.
相關臨床試驗
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相關器械（代碼：DRG）
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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