Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in ItalyLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Interlab S.R.L. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Jun 30, 2006: MICROGEL ALKALINE HEMOGLOBIN ELECTROPHORESIS TEST SYSTEM, MICROGEL ACID HEMOGLOBIN ELECT….
| Date | Record | Source |
|---|---|---|
| Jun 30, 2006 | MICROGEL ALKALINE HEMOGLOBIN ELECTROPHORESIS TEST SYSTEM, MICROGEL ACID HEMOGLOBIN ELECTROPHORESIS TEST SYSTEMK053571 · JBD | 510(k) clearances |
| May 4, 2004 | INTERLAB ACID HEMOGLOBIN ELECTROPHORESIS TEST SYSTEMK040146 · GKA | 510(k) clearances |
| Feb 3, 2004 | INTERLAB ALKALINE HEMOGLOBIN ELECTROPHORESIS TEST SYSTEMK032862 · JBD | 510(k) clearances |
| Nov 19, 2003 | INTERLAB IMMUNOFIXATION TEST(S)K033187 · CFF | 510(k) clearances |
| Sep 13, 1985 | 600/L 5X6' UVA 85W LAMPS, 5X5 UVA 65W LAMPS 500/LK853394 · FTC | 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
