# Labsystems, Inc.

- Location (FDA's records): Morton Grove, IL
- FDA decisions: 17 (1984–1993): 17 510(k) clearances
- Product codes: LFX (5), LGD (5), GQI (2), JJQ (2), JJE (1), ITI (1), KHE (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
- K923365: Tilt/Reduced Shear Semi-Recline Seating System (Mar 24, 1993)
- K896474: Resubmitted Fecatwin Sensitive - Feca-Eia (Jan 25, 1990)
- K890154: Modified Labysystems' Toxoplasma Gondii Igg Eia (Feb 7, 1989)
- K890091: Modified Labsystems' Rubella Igg Eia Test Kit (Feb 3, 1989)
- K881243: Rubella Igg - Eia Test Kit Number 61 07 201 (Apr 4, 1988)
- K873780: Modification Rubella Igm Eia Test Kit (Oct 15, 1987)
- K873583: Auto-Eia (Sep 22, 1987)
- K872252: Modified Toxoplasma Gondii Igg Eia Test Kit (Jul 1, 1987)

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