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FDA 510(k)

梅克爾緊急氣管切开針套組,梅克爾通用氣管切开針套組

K 號:K160200 · 2017-02-17

決定日期2017-02-17
產品代碼BWC
諮詢委員會AN
決定相當於

器材摘要

Melker Cuffed Emergency Cricothyrotomy Catheter Sets, Melker Universal Cricothyrotomy Catheter Set is the device name listed in this FDA 510(k) record. The listed applicant is Cook Incorporated. It received FDA 510(k) clearance on 2017-02-17 under 510(k) number K160200. The device is classified under product code BWC. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Melker Cuffed Emergency Cricothyrotomy Catheter Sets, Melker Universal Cricothyrotomy Catheter Set?

Melker Cuffed Emergency Cricothyrotomy Catheter Sets, Melker Universal Cricothyrotomy Catheter Set is a medical device that received FDA 510(k) clearance on 2017-02-17. The listed applicant is Cook Incorporated. The 510(k) number is K160200.

When did Melker Cuffed Emergency Cricothyrotomy Catheter Sets, Melker Universal Cricothyrotomy Catheter Set receive FDA 510(k) clearance?

Melker Cuffed Emergency Cricothyrotomy Catheter Sets, Melker Universal Cricothyrotomy Catheter Set received FDA 510(k) clearance on 2017-02-17, under 510(k) number K160200.

Who is the listed applicant for Melker Cuffed Emergency Cricothyrotomy Catheter Sets, Melker Universal Cricothyrotomy Catheter Set?

The FDA 510(k) record lists Cook Incorporated as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Melker Cuffed Emergency Cricothyrotomy Catheter Sets, Melker Universal Cricothyrotomy Catheter Set?

The FDA product code for Melker Cuffed Emergency Cricothyrotomy Catheter Sets, Melker Universal Cricothyrotomy Catheter Set is BWC.

相關臨床試驗

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其他以 Cook Incorporated 為申請人之記錄

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相關器械(代碼:BWC)

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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