3 devices · 1 company · 2020 to 2024
Limbus AI Inc.: AI-enabled devices on FDA's list
3 devices from Limbus AI Inc., 2020 to 2024, from 1 company across 2 product codes. Each record carries FDA's decision, the Indications for Use statement verbatim where the public document carries one (3 of 3 here), the regulation, and MAUDE report counts by product code.
Retrieved from FDA public records.
Product codes from Limbus AI Inc.
Every device, newest decision first
| Decision | Device | Panel | Product code | FDA |
|---|---|---|---|---|
| Limbus ContourK241837 · 510(k) | Radiology | QKB | database entry | |
| Limbus ContourK230575 · 510(k) | Radiology | LLZ | database entry | |
| Limbus ContourK201232 · 510(k) | Radiology | LLZ | database entry |
Every company in the record, the whole record of FDA AI-enabled medical devices, or what Apodicta does on a medical record.