Qure.Ai Technologies
IndiaFDA 510(k) applicant, unverified
- Devices
- 9
What Qure.Ai Technologies makes
Qure.Ai Technologies develops AI-powered diagnostic imaging solutions, including automated analysis tools for lung nodules (qXR-LN, qXR-CTR, qXR-Detect), pulmonary embolism detection (qXR-PTX-PE), and emergency radiology (qER, qER-Quant). Their portfolio also covers quantitative imaging metrics for lung nodules (qCT LN Quant) and emergency CT angiography (qER-CTA).
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearance pathways. The company is headquartered in the United States.
Catalogue
qXR-LN Ref K231805
510(k) 510(k)qXR-CTR Ref K231149
510(k) 510(k)qER Ref K200921
510(k) 510(k)qXR-BT Ref K212690
510(k) 510(k)qXR-PTX-PE Ref K230899
510(k) 510(k)qXR-Detect Ref K251934
510(k) 510(k)qCT LN Quant Ref K240740
510(k) 510(k)qER-Quant Ref K211222
510(k) 510(k)qER-CTA (v1.0) Ref K251610
510(k) 510(k)
Frequently asked questions
How many devices does Qure.Ai Technologies have in the registry?
The registry currently lists 9 devices for Qure.Ai Technologies. Devices recorded under merged duplicate company entries are counted once.
Which registries list Qure.Ai Technologies's devices?
Among its 9 most recently registered devices, Qure.Ai Technologies has devices listed in FDA 510(k) (9 devices).
What risk classes do Qure.Ai Technologies's devices fall under?
Among its 9 most recently registered devices, the classes recorded for Qure.Ai Technologies's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Qure.Ai Technologies in the registry?
The most recently registered devices listed for Qure.Ai Technologies include qXR-LN, qXR-CTR, qER and qXR-BT.