FDA 510(k)

Oxus筛床

K号: K211056 · 2023-05-31

决定日期2023-05-31

产品代码CAW

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决定实质等同

器械摘要

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.

常见问题

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.

列明Oxus, Inc.为申报人的其他记录

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。

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