FDA 510(k)

Oxus 絞網床

K 號：K211056 · 2023-05-31

決定日期2023-05-31

產品代碼CAW

諮詢委員會AN

決定相當於

器材摘要

Oxus Sieve Beds is the device name listed in this FDA 510(k) record. The listed applicant is Oxus, Inc.. It received FDA 510(k) clearance on 2023-05-31 under 510(k) number K211056. 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 Oxus Sieve Beds?

Oxus Sieve Beds is a medical device that received FDA 510(k) clearance on 2023-05-31. The listed applicant is Oxus, Inc.. The 510(k) number is K211056.

When did Oxus Sieve Beds receive FDA 510(k) clearance?

Oxus Sieve Beds received FDA 510(k) clearance on 2023-05-31, under 510(k) number K211056.

Who is the listed applicant for Oxus Sieve Beds?

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

What is the FDA product code for Oxus Sieve Beds?

The FDA product code for Oxus Sieve Beds is CAW.

其他以 Oxus, Inc. 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。

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官方來源

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