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FDA 510(k)

CogNet QmTRIAGE

K-Number: K220080 · 2022-09-29

ApplicantMedcognetics, Inc.
Decision Date2022-09-29
Product CodeQFM
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CogNet QmTRIAGE is a medical device manufactured by Medcognetics, Inc.. It received FDA 510(k) clearance on 2022-09-29 under approval number K220080. The device is classified under product code QFM. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CogNet QmTRIAGE?

CogNet QmTRIAGE is a medical device that received FDA 510(k) clearance on 2022-09-29. It is manufactured by Medcognetics, Inc.. The 510(k) number is K220080.

When was CogNet QmTRIAGE approved by the FDA?

CogNet QmTRIAGE received FDA 510(k) clearance on 2022-09-29, under approval number K220080.

What company makes CogNet QmTRIAGE?

CogNet QmTRIAGE is manufactured by Medcognetics, Inc..

What is the FDA product code for CogNet QmTRIAGE?

The FDA product code for CogNet QmTRIAGE is QFM.

Other Devices by Medcognetics, Inc.

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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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