SIDDHARTH-II；影響
K 號：K222762 · 2023-06-08
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器材摘要
SIDDHARTH-II;IMPACT is the device name listed in this FDA 510(k) record. The listed applicant is Panacea Medical Technologies Pvt. , Ltd.. It received FDA 510(k) clearance on 2023-06-08 under 510(k) number K222762. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the SIDDHARTH-II;IMPACT?
SIDDHARTH-II;IMPACT is a medical device that received FDA 510(k) clearance on 2023-06-08. The listed applicant is Panacea Medical Technologies Pvt. , Ltd.. The 510(k) number is K222762.
When did SIDDHARTH-II;IMPACT receive FDA 510(k) clearance?
SIDDHARTH-II;IMPACT received FDA 510(k) clearance on 2023-06-08, under 510(k) number K222762.
Who is the listed applicant for SIDDHARTH-II;IMPACT?
The FDA 510(k) record lists Panacea Medical Technologies Pvt. , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SIDDHARTH-II;IMPACT?
The FDA product code for SIDDHARTH-II;IMPACT is IYE.
相關臨床試驗
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其他以 Panacea Medical Technologies Pvt. , Ltd. 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。
相關器械（代碼：IYE）
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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