Oxus Sieve Beds
K-Number: K211056 · 2023-05-31
Device Summary
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. 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.
Other records listing Oxus, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: CAW)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.