ZIIP+ 裝置
K 號：K212342 · 2021-09-23
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器材摘要
ZIIP+ Device is the device name listed in this FDA 510(k) record. The listed applicant is Ziip, Inc.. It received FDA 510(k) clearance on 2021-09-23 under 510(k) number K212342. The device is classified under product code NFO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the ZIIP+ Device?
ZIIP+ Device is a medical device that received FDA 510(k) clearance on 2021-09-23. The listed applicant is Ziip, Inc.. The 510(k) number is K212342.
When did ZIIP+ Device receive FDA 510(k) clearance?
ZIIP+ Device received FDA 510(k) clearance on 2021-09-23, under 510(k) number K212342.
Who is the listed applicant for ZIIP+ Device?
The FDA 510(k) record lists Ziip, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ZIIP+ Device?
The FDA product code for ZIIP+ Device is NFO.
相關臨床試驗
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相關器械（代碼：NFO）
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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