Endolumik 胃道校準管 M 系列型號 (EGCT36M)；Endolumik 胃道校準管 M 系列型號 (EGCT40M)
K 號：K240069 · 2024-02-08
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器材摘要
常見問題
What is the Endolumik Gastric Calibration Tube M Series (EGCT36M); Endolumik Gastric Calibration Tube M Series (EGCT40M)?
Endolumik Gastric Calibration Tube M Series (EGCT36M); Endolumik Gastric Calibration Tube M Series (EGCT40M) is a medical device that received FDA 510(k) clearance on 2024-02-08. The listed applicant is Endolumik. The 510(k) number is K240069.
When did Endolumik Gastric Calibration Tube M Series (EGCT36M); Endolumik Gastric Calibration Tube M Series (EGCT40M) receive FDA 510(k) clearance?
Endolumik Gastric Calibration Tube M Series (EGCT36M); Endolumik Gastric Calibration Tube M Series (EGCT40M) received FDA 510(k) clearance on 2024-02-08, under 510(k) number K240069.
Who is the listed applicant for Endolumik Gastric Calibration Tube M Series (EGCT36M); Endolumik Gastric Calibration Tube M Series (EGCT40M)?
The FDA 510(k) record lists Endolumik as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Endolumik Gastric Calibration Tube M Series (EGCT36M); Endolumik Gastric Calibration Tube M Series (EGCT40M)?
The FDA product code for Endolumik Gastric Calibration Tube M Series (EGCT36M); Endolumik Gastric Calibration Tube M Series (EGCT40M) is KNT.
相關臨床試驗
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相關器械（代碼：KNT）
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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