Wieslab AB
FDA 510(k) & PMA Approved Devices — 5 products
Advertisement
Total Devices5
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K981748 | WIELISA ANCA SCREENING KIT TEST SYSTEM | MOB | 1998-07-22 | View |
| 510(k) | K981750 | WIELISA ANTI-GBM, ANCA SCREENING KIT TEST SYSTEM | MOB | 1998-07-22 | View |
| 510(k) | K974167 | WIELISA PR-3 ANCA TEST SYSTEM | MOB | 1998-02-17 | View |
| 510(k) | K974169 | WIELISA ANTI-GBM TEST SYSTEM | DBL | 1998-02-17 | View |
| 510(k) | K974166 | WIELISA MPO ANCA TEST SYSTEM | MOB | 1998-02-17 | View |
No matching devices.
Advertisement