Spirotome Endo 08 肠道刀，Spirotome Endo 10 肠道刀，Spirotome Endo 14 肠道刀，配 10 mm 鋸齒的 Spirotome Endo 14 肠道刀
K 號：K190378 · 2019-05-24
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器材摘要
常見問題
What is the Spirotome Endo 08 Gauge, Spirotome Endo 10 Gauge, Spirotome Endo 14 Gauge, Spirotome Endo 14 Gauge with 10 mm Helix?
Spirotome Endo 08 Gauge, Spirotome Endo 10 Gauge, Spirotome Endo 14 Gauge, Spirotome Endo 14 Gauge with 10 mm Helix is a medical device that received FDA 510(k) clearance on 2019-05-24. The listed applicant is Bioncise NV. The 510(k) number is K190378.
When did Spirotome Endo 08 Gauge, Spirotome Endo 10 Gauge, Spirotome Endo 14 Gauge, Spirotome Endo 14 Gauge with 10 mm Helix receive FDA 510(k) clearance?
Spirotome Endo 08 Gauge, Spirotome Endo 10 Gauge, Spirotome Endo 14 Gauge, Spirotome Endo 14 Gauge with 10 mm Helix received FDA 510(k) clearance on 2019-05-24, under 510(k) number K190378.
Who is the listed applicant for Spirotome Endo 08 Gauge, Spirotome Endo 10 Gauge, Spirotome Endo 14 Gauge, Spirotome Endo 14 Gauge with 10 mm Helix?
The FDA 510(k) record lists Bioncise NV as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Spirotome Endo 08 Gauge, Spirotome Endo 10 Gauge, Spirotome Endo 14 Gauge, Spirotome Endo 14 Gauge with 10 mm Helix?
The FDA product code for Spirotome Endo 08 Gauge, Spirotome Endo 10 Gauge, Spirotome Endo 14 Gauge, Spirotome Endo 14 Gauge with 10 mm Helix 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。
官方來源
在 FDA 資料庫中查看 →資料來源為 FDA Open API。如需最新且權威的資訊，請始終參閱官方記錄。
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