CogNet AI-MT+
FDA 510(k) K252482 · Medcognetics, Inc.
510(k) numberK252482
Submission
- Device name
- CogNet AI-MT+
- Applicant
- Medcognetics, Inc.
Dallas, TX, US - Received
- August 7, 2025
- Decision date
- December 11, 2025
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- QFM – Radiological Computer-Assisted Prioritization Software For Lesions
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 892.2080
- Specialty
- Radiology
Radiological computer-assisted prioritization software for lesions is an image processing device intended to aid in prioritization and triage of time sensitive patient detection and diagnosis based on the analysis of medical images acquired from radiological signal acquisition systems. The device identifies or prioritizes time sensitive imaging for review by prespecified clinical users based on…
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|---|---|---|---|
| K253751 | CXRDetectAIQFM · Traditional | Neurocareai, Inc. (Dba Savelife.Ai) | 07/08/2026SE |
| K252954 | MammoSightAIQFM · Traditional | Neurocareai, Inc. (Dba Savelife.Ai) | 05/04/2026SE |
| K250831 | Annalise EnterpriseQFM · Special | Annalise-Ai | 04/23/2025SE |
| K243808 | Rayvolve PTX-PEQFM · Traditional | AZmed | 03/21/2025SE |
| K243548 | BriefCase-TriageQFM · Special | Aidoc Medical , Ltd. | 12/11/2024SE |
| K241439 | VUNO Med-Chest X-ray Triage/VUNO Med-CXR Link TriageQFM · Traditional | Vuno, Inc. | 11/15/2024SE |
| K240612 | Cina-VcfQFM · Traditional | Avicenna.Ai | 05/31/2024SE |
| K233108 | VinDr-MammoQFM · Traditional | Vinbigdata Joint Stock Company | 05/23/2024SE |
| K232410 | SmartChestQFM · Traditional | Milvue | 05/10/2024SE |
| K231871 | Radify TriageQFM · Abbreviated | Envisionit Deepai, Ltd. | 01/17/2024SE |
More from Envisionit Deepai, Ltd.
| 510(k) | Device | Decision |
|---|---|---|
| K220080 | CogNet QmTRIAGEQFM · Traditional | 09/29/2022SE |
Questions and answers
When was CogNet AI-MT+ cleared by the FDA?
CogNet AI-MT+ (K252482) received a 510(k) decision of Substantially Equivalent on December 11, 2025, 126 days after the submission was received.
What is the product code of K252482?
The FDA product code is QFM – Radiological Computer-Assisted Prioritization Software For Lesions, a Class II (moderate risk) device regulated under 21 CFR 892.2080.