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FDA 510(k)

Invacare 銀河系列移動氧氣濃縮器

K 號:K160630 · 2016-09-27

決定日期2016-09-27
產品代碼CAW
諮詢委員會AN
決定相當於

器材摘要

Invacare Platinum Mobile 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 2016-09-27 under 510(k) number K160630. 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 Mobile Oxygen Concentrator?

Invacare Platinum Mobile Oxygen Concentrator is a medical device that received FDA 510(k) clearance on 2016-09-27. The listed applicant is Invacare Corporation. The 510(k) number is K160630.

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

Invacare Platinum Mobile Oxygen Concentrator received FDA 510(k) clearance on 2016-09-27, under 510(k) number K160630.

Who is the listed applicant for Invacare Platinum Mobile 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 Mobile Oxygen Concentrator?

The FDA product code for Invacare Platinum Mobile 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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