Epocal, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest FDA decision2020-06-05
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K200107 | epoc Blood Analysis System | CHL | 2020-06-05 | View |
| 510(k) | K171247 | epoc Blood Urea Nitrogen Test, epoc Total Carbon Dioxide Test | CDS | 2018-01-17 | View |
No matching devices.