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FDA 510(k)

vRad Viewer

K-Number: K241879 · 2024-07-18

ApplicantVirtual Radiologic Corporation
Decision Date2024-07-18
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

vRad Viewer is a medical device manufactured by Virtual Radiologic Corporation. It received FDA 510(k) clearance on 2024-07-18 under approval number K241879. 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 vRad Viewer?

vRad Viewer is a medical device that received FDA 510(k) clearance on 2024-07-18. It is manufactured by Virtual Radiologic Corporation. The 510(k) number is K241879.

When was vRad Viewer approved by the FDA?

vRad Viewer received FDA 510(k) clearance on 2024-07-18, under approval number K241879.

What company makes vRad Viewer?

vRad Viewer is manufactured by Virtual Radiologic Corporation.

What is the FDA product code for vRad Viewer?

The FDA product code for vRad Viewer is LLZ.

Other Devices by Virtual Radiologic Corporation

K162145vRad PACS with Mammography

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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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