Wieslab AB
Wieslab AB appears in FDA public data with 0 recalls, 5 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on July 22, 1998.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K981750 | WIELISA ANTI-GBM, ANCA SCREENING KIT TEST SYSTEM | July 22, 1998 |
| K981748 | WIELISA ANCA SCREENING KIT TEST SYSTEM | July 22, 1998 |
| K974169 | WIELISA ANTI-GBM TEST SYSTEM | February 17, 1998 |
| K974167 | WIELISA PR-3 ANCA TEST SYSTEM | February 17, 1998 |
| K974166 | WIELISA MPO ANCA TEST SYSTEM | February 17, 1998 |