# Interlab S.R.L.

- Location (FDA's records): East Stroudsburg, PA
- FDA decisions: 4 (2003–2006): 4 510(k) clearances
- Product codes: JBD (2), GKA (1), CFF (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K053571: Microgel Alkaline Hemoglobin Electrophoresis Test System, Microgel Acid Hemoglobin Electrophoresis Test System (Jun 30, 2006)
- K040146: Interlab Acid Hemoglobin Electrophoresis Test System (May 4, 2004)
- K032862: Interlab Alkaline Hemoglobin Electrophoresis Test System (Feb 3, 2004)
- K033187: Interlab Immunofixation Test (S) (Nov 19, 2003)

Source page: https://510kreport.com/company/interlab