Helena Laboratories, Corp.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest FDA decision2022-10-13
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K213396 | SPIFE A1AT kit | OBZ | 2022-10-13 | View |
| 510(k) | K192931 | V8 Nexus Hemoglobin Ultrascreen, V8 AFSA2 Hemo Control | GKA | 2022-04-19 | View |
No matching devices.