5 devices · 3 companies · 2023 to 2026
Neurophet., Inc.: AI-enabled devices on FDA's list
5 devices from Neurophet., Inc., 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 (5 of 5 here), the regulation, and MAUDE report counts by product code.
Retrieved from FDA public records.
Product codes from Neurophet., Inc.
Every device, newest decision first
| Decision | Device | Panel | Product code | FDA |
|---|---|---|---|---|
| Neurophet SCALE PETK252563 · 510(k) | Radiology | QIH | database entry | |
| Neurophet AQUAK261273 · 510(k) | Radiology | QIH | database entry | |
| Neurophet AQUA AD PlusK252496 · 510(k) | Radiology | QIH | database entry | |
| Neurophet AQUAK242215 · 510(k) | Radiology | QIH | database entry | |
| Neurophet AQUAK220437 · 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.