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FDA 510(k)

Xoran Workstation, Model 10050

K-Number: K210257 · 2021-05-20

ApplicantXoran Technologies, LLC
Decision Date2021-05-20
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Xoran Workstation, Model 10050 is the device name listed in this FDA 510(k) record. The listed applicant is Xoran Technologies, LLC. It received FDA 510(k) clearance on 2021-05-20 under 510(k) number K210257. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Xoran Workstation, Model 10050?

Xoran Workstation, Model 10050 is a medical device that received FDA 510(k) clearance on 2021-05-20. The listed applicant is Xoran Technologies, LLC. The 510(k) number is K210257.

When did Xoran Workstation, Model 10050 receive FDA 510(k) clearance?

Xoran Workstation, Model 10050 received FDA 510(k) clearance on 2021-05-20, under 510(k) number K210257.

Who is the listed applicant for Xoran Workstation, Model 10050?

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

What is the FDA product code for Xoran Workstation, Model 10050?

The FDA product code for Xoran Workstation, Model 10050 is LLZ.

Other records listing Xoran Technologies, LLC 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.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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