Helix Opco, LLC
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest Approval2020-12-23
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K192073 | Helix Genetic Health Risk App for late-onset Alzheimers disease | PTA | 2020-12-23 | View |
| 510(k) | DEN190035 | Helix Laboratory Platform | QNC | 2020-12-23 | View |
No matching devices.