Company ยท US
Wieslab AB
FDA 510(k) clearances and medical device recalls filed under this name, 1998 to 1998. Name variants (Inc, Corp, punctuation) are merged.
5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Jul 22, 1998 | K981750 | WIELISA ANTI-GBM, ANCA SCREENING KIT TEST SYSTEM Wieslab AB | MOB |
| Jul 22, 1998 | K981748 | WIELISA ANCA SCREENING KIT TEST SYSTEM Wieslab AB | MOB |
| Feb 17, 1998 | K974169 | WIELISA ANTI-GBM TEST SYSTEM Wieslab AB | DBL |
| Feb 17, 1998 | K974167 | WIELISA PR-3 ANCA TEST SYSTEM Wieslab AB | MOB |
| Feb 17, 1998 | K974166 | WIELISA MPO ANCA TEST SYSTEM Wieslab AB | MOB |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||