# K220080: CogNet QmTRIAGE

- Pathway: 510(k) (Traditional)
- Applicant: Medcognetics, Inc.
- Decided: Sep 29, 2022 after 262 days
- Product code: QFM (Radiological Computer-Assisted Prioritization Software For Lesions)
- Device class: 2
- Regulation: 21 CFR 892.2080
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 3 generations back to DEN170073 (2018). 3 ancestors in all.
2 later devices descend from it; 2 cite it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K200905: HealthMammo, Zebra Medical Vision, Ltd. (2020) Summary page 4.

## Most influential descendants
- K252482: CogNet AI-MT+ (2025), 0 descendants of its own
- K233108: VinDr-Mammo (2024), 0 descendants of its own

## Indications for use
The MedCognetics (CogNet) QmTRIAGE TM software is a passive notification for prioritization-only, parallel-workflow software tool used by MQSA qualified interpreting physicians to prioritize patients with suspicious findings in the medical care environment. QmTRIAGETM utilizes an artificial intelligence algorithm to analyze 2D FFDM screening mammograms and flags those that are suggestive of the presence ofat least one suspicious finding at the exam level. QmTRIAGE TM produces an exam level output to a PACS/Workstation for flagging the suspicious study and allows for worklist prioritization. MQSA qualified interpreting physicians are responsible for reviewing each exam on a display approved for use in mammography, according to the current standard of care. The QmTRIAGETm device is limited to the categorization of exams, does not provide any diagnostic information beyond triage and prioritization, does not remove images from the interpreting physician's worklist, and should not be used in lieu of full patient evaluation, or relied upon to make or confirm diagnosis. The QmTRIAGETM device is intended for use with complete 2D FFDM mammography exams acquired using validated FFDM systems only.

Source page: https://510kreport.com/device/K220080
Methodology: https://510kreport.com/methodology