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FDA 510(k)

XVIEWNET

K-Number: K080290 · 2008-02-22

ApplicantAmerican Radiologist Network, Inc.
Decision Date2008-02-22
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

XVIEWNET is the device name listed in this FDA 510(k) record. The listed applicant is American Radiologist Network, Inc.. It received FDA 510(k) clearance on 2008-02-22 under 510(k) number K080290. 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 XVIEWNET?

XVIEWNET is a medical device that received FDA 510(k) clearance on 2008-02-22. The listed applicant is American Radiologist Network, Inc.. The 510(k) number is K080290.

When did XVIEWNET receive FDA 510(k) clearance?

XVIEWNET received FDA 510(k) clearance on 2008-02-22, under 510(k) number K080290.

Who is the listed applicant for XVIEWNET?

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

What is the FDA product code for XVIEWNET?

The FDA product code for XVIEWNET is LLZ.

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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.

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