FDA 510(k)

Invacare AVIVA FX 電動輪椅，型號：IFX-20MP

K 號：K192216 · 2020-01-02

決定日期2020-01-02

產品代碼ITI

諮詢委員會PM

決定相當於

器材摘要

Invacare AVIVA FX Power Wheelchair, Model: IFX-20MP is the device name listed in this FDA 510(k) record. The listed applicant is Invacare Corporation. It received FDA 510(k) clearance on 2020-01-02 under 510(k) number K192216. The device is classified under product code ITI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Invacare AVIVA FX Power Wheelchair, Model: IFX-20MP?

Invacare AVIVA FX Power Wheelchair, Model: IFX-20MP is a medical device that received FDA 510(k) clearance on 2020-01-02. The listed applicant is Invacare Corporation. The 510(k) number is K192216.

When did Invacare AVIVA FX Power Wheelchair, Model: IFX-20MP receive FDA 510(k) clearance?

Invacare AVIVA FX Power Wheelchair, Model: IFX-20MP received FDA 510(k) clearance on 2020-01-02, under 510(k) number K192216.

Who is the listed applicant for Invacare AVIVA FX Power Wheelchair, Model: IFX-20MP?

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

What is the FDA product code for Invacare AVIVA FX Power Wheelchair, Model: IFX-20MP?

The FDA product code for Invacare AVIVA FX Power Wheelchair, Model: IFX-20MP is ITI.

其他以 Invacare Corporation 為申請人之記錄

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相關器械（代碼：ITI）

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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官方來源

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