TAP 鋸片
K 號：K223201 · 2023-04-19
廣告
器材摘要
TAP Lancet is the device name listed in this FDA 510(k) record. The listed applicant is Yourbio Health, Inc.. It received FDA 510(k) clearance on 2023-04-19 under 510(k) number K223201. The device is classified under product code FMK. It was reviewed by the SU advisory panel. FDA Decision: Unknown.
常見問題
What is the TAP Lancet?
TAP Lancet is a medical device that received FDA 510(k) clearance on 2023-04-19. The listed applicant is Yourbio Health, Inc.. The 510(k) number is K223201.
When did TAP Lancet receive FDA 510(k) clearance?
TAP Lancet received FDA 510(k) clearance on 2023-04-19, under 510(k) number K223201.
Who is the listed applicant for TAP Lancet?
The FDA 510(k) record lists Yourbio Health, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TAP Lancet?
The FDA product code for TAP Lancet is FMK.
相關臨床試驗
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：FMK）
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。
K262526安全針 (XL)Tianjin Huahong Technology Co., Ltd.K261045驗精安全針Promisemed Hangzhou Meditech Co., Ltd.K260191安全針刺器（XXXVII）Tianjin Huahong Technology Co., Ltd.K253605安全針刺針Ningbo Medsun Medical Co., Ltd.K252490足跟針安全針筒（HHZ-II，HHZ-III，HHZ-IV）Tianjin Huahong Technology Co., Ltd.K251694安全針Tianjin Huahong Technology Co., Ltd.
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。
廣告