TeesuVac 乳癌切片儀型號 1
K 號：K212079 · 2022-02-02
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器材摘要
TeesuVac Breast Biopsy Device Mark 1 is the device name listed in this FDA 510(k) record. The listed applicant is Teesuvac Aps. It received FDA 510(k) clearance on 2022-02-02 under 510(k) number K212079. The device is classified under product code KNW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the TeesuVac Breast Biopsy Device Mark 1?
TeesuVac Breast Biopsy Device Mark 1 is a medical device that received FDA 510(k) clearance on 2022-02-02. The listed applicant is Teesuvac Aps. The 510(k) number is K212079.
When did TeesuVac Breast Biopsy Device Mark 1 receive FDA 510(k) clearance?
TeesuVac Breast Biopsy Device Mark 1 received FDA 510(k) clearance on 2022-02-02, under 510(k) number K212079.
Who is the listed applicant for TeesuVac Breast Biopsy Device Mark 1?
The FDA 510(k) record lists Teesuvac Aps as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TeesuVac Breast Biopsy Device Mark 1?
The FDA product code for TeesuVac Breast Biopsy Device Mark 1 is KNW.
相關臨床試驗
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相關器械（代碼：KNW）
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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