MyOn HC 電動輪椅
K 號：K152536 · 2016-01-05
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器材摘要
MyOn HC Manual Wheelchair is the device name listed in this FDA 510(k) record. The listed applicant is Invacare Corporation. It received FDA 510(k) clearance on 2016-01-05 under 510(k) number K152536. The device is classified under product code IOR. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the MyOn HC Manual Wheelchair?
MyOn HC Manual Wheelchair is a medical device that received FDA 510(k) clearance on 2016-01-05. The listed applicant is Invacare Corporation. The 510(k) number is K152536.
When did MyOn HC Manual Wheelchair receive FDA 510(k) clearance?
MyOn HC Manual Wheelchair received FDA 510(k) clearance on 2016-01-05, under 510(k) number K152536.
Who is the listed applicant for MyOn HC Manual Wheelchair?
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 MyOn HC Manual Wheelchair?
The FDA product code for MyOn HC Manual Wheelchair is IOR.
相關臨床試驗
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其他以 Invacare Corporation 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。
相關器械（代碼：IOR）
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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