FDA 510(k)

IDENTIFY

K-Number: K192968 · 2019-11-12

Decision Date2019-11-12

Product CodeIYE

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

IDENTIFY is a medical device manufactured by Varian Medical Systems, Inc.. It received FDA 510(k) clearance on 2019-11-12 under approval number K192968. 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 IDENTIFY?

IDENTIFY is a medical device that received FDA 510(k) clearance on 2019-11-12. It is manufactured by Varian Medical Systems, Inc.. The 510(k) number is K192968.

When was IDENTIFY approved by the FDA?

IDENTIFY received FDA 510(k) clearance on 2019-11-12, under approval number K192968.

What company makes IDENTIFY?

IDENTIFY is manufactured by Varian Medical Systems, Inc..

What is the FDA product code for IDENTIFY?

The FDA product code for IDENTIFY 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.