6 devices · 2 companies · 2023

Annalise-AI Pty Ltd: AI-enabled devices on FDA's list

6 devices from Annalise-AI Pty Ltd, 2023, from 2 companies across 2 product codes. Each record carries FDA's decision, the Indications for Use statement verbatim where the public document carries one (6 of 6 here), the regulation, and MAUDE report counts by product code.

Retrieved from FDA public records.

Product codes from Annalise-AI Pty Ltd

Every device, newest decision first

Annalise-AI Pty Ltd · 6 devices
DecisionDevicePanelProduct codeFDA
Annalise Enterprise CTB Triage TraumaK231767 · 510(k)RadiologyQASdatabase entry
Annalise Enterprise CTB Triage TraumaK231384 · 510(k)RadiologyQASdatabase entry
Annalise Enterprise CTB Triage-OHK231094 · 510(k)RadiologyQASdatabase entry
Annalise Enterprise CTB Triage TraumaK223240 · 510(k)RadiologyQASdatabase entry
Annalise Enterprise CXR Triage TraumaK222179 · 510(k)RadiologyQFMdatabase entry
Annalise Enterprise CXR Triage TraumaK222268 · 510(k)RadiologyQFMdatabase entry

Every company in the record, the whole record of FDA AI-enabled medical devices, or what Apodicta does on a medical record.

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Every device here is authorized for a stated use. See a record read against what it must prove, on your own file.

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