Diagnostics makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in SwedenLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Wieslab with 5 510(k) clearances. The most recent is a 510(k) clearance dated Jul 22, 1998: WIELISA ANTI-GBM, ANCA SCREENING KIT TEST SYSTEM.
| Jul 22, 1998 | WIELISA ANTI-GBM, ANCA SCREENING KIT TEST SYSTEMK981750 · MOB | 510(k) clearances |
| Jul 22, 1998 | WIELISA ANCA SCREENING KIT TEST SYSTEMK981748 · MOB | 510(k) clearances |
| Feb 17, 1998 | WIELISA MPO ANCA TEST SYSTEMK974166 · MOB | 510(k) clearances |
| Feb 17, 1998 | WIELISA ANTI-GBM TEST SYSTEMK974169 · DBL | 510(k) clearances |
| Feb 17, 1998 | WIELISA PR-3 ANCA TEST SYSTEMK974167 · MOB | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
