3 devices · 1 company · 2018 to 2020
Oculogica, Inc.: AI-enabled devices on FDA's list
3 devices from Oculogica, Inc., 2018 to 2020, from 1 company across 1 product code. 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.
Every device, newest decision first
| Decision | Device | Panel | Product code | FDA |
|---|---|---|---|---|
| EyeBOXK201841 · 510(k) | Neurology | QEA | database entry | |
| EyeBOXK191183 · 510(k) | Neurology | QEA | database entry | |
| EyeBOXDEN170091 · De Novo | Neurology | QEA | database entry |
Every company in the record, the whole record of FDA AI-enabled medical devices, or what Apodicta does on a medical record.