# Concord Laboratories, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 42 (1976–1989): 42 510(k) clearances
- Product codes: FMF (6), FCM (5), KNX (5), CBT (4), LKB (3), CAZ (3), BSY (3), GCB (1), FNY (1), FMC (1), GJE (1), HXD (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
- K883840: Dri-Vent Arterial Blood Sampling Kit (May 16, 1989)
- K871825: Meconium Suction Catheter (Jun 29, 1987)
- K864535: Tracheobronchial Suction Catheter, Cat. NO. 6110 (Jan 6, 1987)
- K862039: Concord Care Tray (Jul 3, 1986)
- K854601: Spring Guide Catheter Anesthesia Conduction Cath (Jan 10, 1986)
- K854327: Subcutaneous Tunneling Needles & Handles (Nov 13, 1985)
- K851134: Regional Anesthesia Trays (Jul 15, 1985)
- K842095: Epidural Trays (Jul 3, 1984)

Source page: https://510kreport.com/company/concord-laboratories
