VPC
K 號：K190345 · 2019-05-16
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器材摘要
VPC is the device name listed in this FDA 510(k) record. The listed applicant is PAJUNK GmbH Medizintechnologie. It received FDA 510(k) clearance on 2019-05-16 under 510(k) number K190345. The device is classified under product code CAZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the VPC?
VPC is a medical device that received FDA 510(k) clearance on 2019-05-16. The listed applicant is PAJUNK GmbH Medizintechnologie. The 510(k) number is K190345.
When did VPC receive FDA 510(k) clearance?
VPC received FDA 510(k) clearance on 2019-05-16, under 510(k) number K190345.
Who is the listed applicant for VPC?
The FDA 510(k) record lists PAJUNK GmbH Medizintechnologie as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VPC?
The FDA product code for VPC is CAZ.
其他以 PAJUNK GmbH Medizintechnologie 為申請人之記錄
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相關器械（代碼：CAZ）
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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