FDA 510(k)

XT系列電動輪椅 (XT2)，XT系列電動輪椅 (XT4)

K 號：K233877 · 2024-03-04

決定日期2024-03-04

產品代碼ITI

諮詢委員會PM

決定相當於

器材摘要

XT Series Power Wheelchair (XT2), XT Series Power Wheelchair (XT4) is the device name listed in this FDA 510(k) record. The listed applicant is Magic Mobility. It received FDA 510(k) clearance on 2024-03-04 under 510(k) number K233877. 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 XT Series Power Wheelchair (XT2), XT Series Power Wheelchair (XT4)?

XT Series Power Wheelchair (XT2), XT Series Power Wheelchair (XT4) is a medical device that received FDA 510(k) clearance on 2024-03-04. The listed applicant is Magic Mobility. The 510(k) number is K233877.

When did XT Series Power Wheelchair (XT2), XT Series Power Wheelchair (XT4) receive FDA 510(k) clearance?

XT Series Power Wheelchair (XT2), XT Series Power Wheelchair (XT4) received FDA 510(k) clearance on 2024-03-04, under 510(k) number K233877.

Who is the listed applicant for XT Series Power Wheelchair (XT2), XT Series Power Wheelchair (XT4)?

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

What is the FDA product code for XT Series Power Wheelchair (XT2), XT Series Power Wheelchair (XT4)?

The FDA product code for XT Series Power Wheelchair (XT2), XT Series Power Wheelchair (XT4) is ITI.

其他以 Magic Mobility 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。

K213090邊疆系列電動輪椅 K211574極端 X8 K203083魔術360電動輪椅

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。

K262582電動輪椅（GP100）Suzhou Green Pine Medical Co., Ltd.K262054電動輪椅Yongkang Joymax Medical Technology Co., Ltd.K260053電動輪椅 (OS-R-M01I)Beijing OrionStar Technology Co., Ltd.K260229電動輪椅（HC819N、HC830N、HC831N）Yongkang Hengyi Vehicle Co., Ltd.K261354電動輪椅（D03）Foshan Sowell Medical Technology Co., Ltd.K261149電動輪椅（DY611A-2，DY612A-1）Zhejiang Lumbre Electric Appliance Co., Ltd.

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。