FDA 510(k)

F&P 850 空氣螺旋成人NIV及NHF電路組套件

K 號：K212031 · 2022-04-22

決定日期2022-04-22

產品代碼BTT

諮詢委員會AN

決定相當於

器材摘要

F&P 850 AirSpiral Adult NIV and NHF Circuit Kit is the device name listed in this FDA 510(k) record. The listed applicant is Fisher & Paykel Healthcare, Ltd.. It received FDA 510(k) clearance on 2022-04-22 under 510(k) number K212031. The device is classified under product code BTT. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the F&P 850 AirSpiral Adult NIV and NHF Circuit Kit?

F&P 850 AirSpiral Adult NIV and NHF Circuit Kit is a medical device that received FDA 510(k) clearance on 2022-04-22. The listed applicant is Fisher & Paykel Healthcare, Ltd.. The 510(k) number is K212031.

When did F&P 850 AirSpiral Adult NIV and NHF Circuit Kit receive FDA 510(k) clearance?

F&P 850 AirSpiral Adult NIV and NHF Circuit Kit received FDA 510(k) clearance on 2022-04-22, under 510(k) number K212031.

Who is the listed applicant for F&P 850 AirSpiral Adult NIV and NHF Circuit Kit?

The FDA 510(k) record lists Fisher & Paykel Healthcare, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for F&P 850 AirSpiral Adult NIV and NHF Circuit Kit?

The FDA product code for F&P 850 AirSpiral Adult NIV and NHF Circuit Kit is BTT.

其他以 Fisher & Paykel Healthcare, Ltd. 為申請人之記錄

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相關器械（代碼：BTT）

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。

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