7 devices · 3 companies · 2023 to 2026

Esaote, S.p.A.: AI-enabled devices on FDA's list

7 devices from Esaote, S.p.A., 2023 to 2026, from 3 companies across 2 product codes. Each record carries FDA's decision, the Indications for Use statement verbatim where the public document carries one (7 of 7 here), the regulation, and MAUDE report counts by product code.

Retrieved from FDA public records.

Product codes from Esaote, S.p.A.

Every device, newest decision first

Esaote, S.p.A. · 7 devices
DecisionDevicePanelProduct codeFDA
6450 Ultrasound SystemK253288 · 510(k)RadiologyIYNdatabase entry
S-scan OpenK260746 · 510(k)RadiologyLNHdatabase entry
Magnifico OpenK251901 · 510(k)RadiologyLNHdatabase entry
7600 Ultrasound SystemK253310 · 510(k)RadiologyIYNdatabase entry
6600 Ultrasound SystemK243253 · 510(k)RadiologyIYNdatabase entry
6450 Ultrasound SystemK241671 · 510(k)RadiologyIYNdatabase entry
6440 MyLabX90K230179 · 510(k)RadiologyIYNdatabase 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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