Zeroveno
K 號：K192337 · 2020-06-22
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器材摘要
Zeroveno is the device name listed in this FDA 510(k) record. The listed applicant is Dimedi Co., Ltd.. It received FDA 510(k) clearance on 2020-06-22 under 510(k) number K192337. The device is classified under product code JOW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Zeroveno?
Zeroveno is a medical device that received FDA 510(k) clearance on 2020-06-22. The listed applicant is Dimedi Co., Ltd.. The 510(k) number is K192337.
When did Zeroveno receive FDA 510(k) clearance?
Zeroveno received FDA 510(k) clearance on 2020-06-22, under 510(k) number K192337.
Who is the listed applicant for Zeroveno?
The FDA 510(k) record lists Dimedi Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Zeroveno?
The FDA product code for Zeroveno is JOW.
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相關器械（代碼：JOW）
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
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