冷凍福
K 號：K170810 · 2017-09-27
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器材摘要
CRYOFOS is the device name listed in this FDA 510(k) record. The listed applicant is Cryofos Medical GmbH. It received FDA 510(k) clearance on 2017-09-27 under 510(k) number K170810. The device is classified under product code GEH. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the CRYOFOS?
CRYOFOS is a medical device that received FDA 510(k) clearance on 2017-09-27. The listed applicant is Cryofos Medical GmbH. The 510(k) number is K170810.
When did CRYOFOS receive FDA 510(k) clearance?
CRYOFOS received FDA 510(k) clearance on 2017-09-27, under 510(k) number K170810.
Who is the listed applicant for CRYOFOS?
The FDA 510(k) record lists Cryofos Medical GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CRYOFOS?
The FDA product code for CRYOFOS is GEH.
相關臨床試驗
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相關器械（代碼：GEH）
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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