Oxus Sieve Beds
K-Number: K211056 · 2023-05-31
ApplicantOxus, Inc.
Decision Date2023-05-31
Product CodeCAW
Advisory CommitteeAN
DecisionSubstantially Equivalent
Device Summary
Oxus Sieve Beds is a medical device manufactured by Oxus, Inc.. It received FDA 510(k) clearance on 2023-05-31 under approval number K211056. The device is classified under product code CAW. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Oxus Sieve Beds?
Oxus Sieve Beds is a medical device that received FDA 510(k) clearance on 2023-05-31. It is manufactured by Oxus, Inc.. The 510(k) number is K211056.
When was Oxus Sieve Beds approved by the FDA?
Oxus Sieve Beds received FDA 510(k) clearance on 2023-05-31, under approval number K211056.
What company makes Oxus Sieve Beds?
Oxus Sieve Beds is manufactured by Oxus, Inc..
What is the FDA product code for Oxus Sieve Beds?
The FDA product code for Oxus Sieve Beds is CAW.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.