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FDA 510(k)

ChitoPulse 9吋 / 23公分,ChitoPulse 12吋 / 30.5公分,ChitoPulse 15吋 / 38公分

K 號:K170958 · 2017-08-29

決定日期2017-08-29
產品代碼DXC
諮詢委員會履歷
決定相當於

器材摘要

ChitoPulse 9in / 23 cm, ChitoPulse 12in / 30.5 cm, ChitoPulse 15in / 38 cm is the device name listed in this FDA 510(k) record. The listed applicant is Tricol Biomedical, Inc.. It received FDA 510(k) clearance on 2017-08-29 under 510(k) number K170958. The device is classified under product code DXC. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the ChitoPulse 9in / 23 cm, ChitoPulse 12in / 30.5 cm, ChitoPulse 15in / 38 cm?

ChitoPulse 9in / 23 cm, ChitoPulse 12in / 30.5 cm, ChitoPulse 15in / 38 cm is a medical device that received FDA 510(k) clearance on 2017-08-29. The listed applicant is Tricol Biomedical, Inc.. The 510(k) number is K170958.

When did ChitoPulse 9in / 23 cm, ChitoPulse 12in / 30.5 cm, ChitoPulse 15in / 38 cm receive FDA 510(k) clearance?

ChitoPulse 9in / 23 cm, ChitoPulse 12in / 30.5 cm, ChitoPulse 15in / 38 cm received FDA 510(k) clearance on 2017-08-29, under 510(k) number K170958.

Who is the listed applicant for ChitoPulse 9in / 23 cm, ChitoPulse 12in / 30.5 cm, ChitoPulse 15in / 38 cm?

The FDA 510(k) record lists Tricol Biomedical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ChitoPulse 9in / 23 cm, ChitoPulse 12in / 30.5 cm, ChitoPulse 15in / 38 cm?

The FDA product code for ChitoPulse 9in / 23 cm, ChitoPulse 12in / 30.5 cm, ChitoPulse 15in / 38 cm is DXC.

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:DXC)

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

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