FDA 510(k)

CogNet QmTRIAGE

K-Number: K220080 · 2022-09-29

Decision Date2022-09-29

Product CodeQFM

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

CogNet QmTRIAGE is the device name listed in this FDA 510(k) record. The listed applicant is Medcognetics, Inc.. It received FDA 510(k) clearance on 2022-09-29 under 510(k) 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. The listed applicant is Medcognetics, Inc.. The 510(k) number is K220080.

When did CogNet QmTRIAGE receive FDA 510(k) clearance?

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

Who is the listed applicant for CogNet QmTRIAGE?

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

What is the FDA product code for CogNet QmTRIAGE?

The FDA product code for CogNet QmTRIAGE is QFM.

Other records listing Medcognetics, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

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