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FDA 510(k)

Invacare 銀河5NXG 氧氣濃縮機

K 號:K203210 · 2021-04-12

決定日期2021-04-12
產品代碼CAW
諮詢委員會AN
決定相當於

器材摘要

Invacare Platinum 5NXG Oxygen Concentrator is the device name listed in this FDA 510(k) record. The listed applicant is Invacare Corporation. It received FDA 510(k) clearance on 2021-04-12 under 510(k) number K203210. The device is classified under product code CAW. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Invacare Platinum 5NXG Oxygen Concentrator?

Invacare Platinum 5NXG Oxygen Concentrator is a medical device that received FDA 510(k) clearance on 2021-04-12. The listed applicant is Invacare Corporation. The 510(k) number is K203210.

When did Invacare Platinum 5NXG Oxygen Concentrator receive FDA 510(k) clearance?

Invacare Platinum 5NXG Oxygen Concentrator received FDA 510(k) clearance on 2021-04-12, under 510(k) number K203210.

Who is the listed applicant for Invacare Platinum 5NXG Oxygen Concentrator?

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 Platinum 5NXG Oxygen Concentrator?

The FDA product code for Invacare Platinum 5NXG Oxygen Concentrator is CAW.

相關臨床試驗

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其他以 Invacare Corporation 為申請人之記錄

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相關器械(代碼:CAW)

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。

官方來源

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