FDA 510(k)

VitalBeam

K-Number: K172013 · 2017-07-28

Decision Date2017-07-28

Product CodeIYE

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

VitalBeam is a medical device manufactured by Varian Medical Systems, Inc.. It received FDA 510(k) clearance on 2017-07-28 under approval number K172013. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VitalBeam?

VitalBeam is a medical device that received FDA 510(k) clearance on 2017-07-28. It is manufactured by Varian Medical Systems, Inc.. The 510(k) number is K172013.

When was VitalBeam approved by the FDA?

VitalBeam received FDA 510(k) clearance on 2017-07-28, under approval number K172013.

What company makes VitalBeam?

VitalBeam is manufactured by Varian Medical Systems, Inc..

What is the FDA product code for VitalBeam?

The FDA product code for VitalBeam is IYE.

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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.