SCS 17-01
K 號：K190956 · 2020-01-30
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器材摘要
SCS 17-01 is the device name listed in this FDA 510(k) record. The listed applicant is Anika Therapeutics, Inc.. It received FDA 510(k) clearance on 2020-01-30 under 510(k) number K190956. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the SCS 17-01?
SCS 17-01 is a medical device that received FDA 510(k) clearance on 2020-01-30. The listed applicant is Anika Therapeutics, Inc.. The 510(k) number is K190956.
When did SCS 17-01 receive FDA 510(k) clearance?
SCS 17-01 received FDA 510(k) clearance on 2020-01-30, under 510(k) number K190956.
Who is the listed applicant for SCS 17-01?
FDA 510(k) 記錄將Anika Therapeutics, Inc. 列為申請人。這並不單獨確立設備製造商。
What is the FDA product code for SCS 17-01?
The FDA product code for SCS 17-01 is MQV.
其他以 Anika Therapeutics, Inc. 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：MQV）
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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