FDA 510(k)

AirSpiral加熱呼吸管

K 號：K162553 · 2018-12-20

決定日期2018-12-20

產品代碼BTT

諮詢委員會AN

決定相當於

器材摘要

AirSpiral Heated Breathing Tube is the device name listed in this FDA 510(k) record. The listed applicant is Fisher & Paykel Healthcare. It received FDA 510(k) clearance on 2018-12-20 under 510(k) number K162553. 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 AirSpiral Heated Breathing Tube?

AirSpiral Heated Breathing Tube is a medical device that received FDA 510(k) clearance on 2018-12-20. The listed applicant is Fisher & Paykel Healthcare. The 510(k) number is K162553.

When did AirSpiral Heated Breathing Tube receive FDA 510(k) clearance?

AirSpiral Heated Breathing Tube received FDA 510(k) clearance on 2018-12-20, under 510(k) number K162553.

Who is the listed applicant for AirSpiral Heated Breathing Tube?

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

What is the FDA product code for AirSpiral Heated Breathing Tube?

The FDA product code for AirSpiral Heated Breathing Tube is BTT.

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

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。

K222292F&P myAirvo 3 K220703F&P 950 呼吸濕化器 K221338F&P空氣輔助3 K162582HumiGard 外科濕化系統，HumiGard 濕化充氣套件

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。

K262268Optiflow 氧氣套件 (AA484J)Fisher and Paykel Healthcare Limited K254078HVT 2.0Vapotherm, Inc.K251448FL-10000U 呼吸濕化器Flexicare Medical Limited.K251419生物加倫尼克實驗室靜脈注射用无菌水，USPLaboratorios Biogalenic S.A. DE C.V.K253479Optiflow Switch+ 過濾鼻接口配二氧化碳採樣功能 (AA042J)Fisher & Paykel Healthcare, Ltd.K250312Hudson RCI® 舒適流鼻管預產期、嬰兒；Hudson RCI® 舒適流 Plus 及軟 Plus 鼻管超小號Medline Industries, LP

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。