# Contour Electrodes, Inc.

- Location (FDA's records): Herrin, IL
- FDA decisions: 4 (1987–1990): 4 510(k) clearances
- Product codes: DRX (3), DRY (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
- K900682: Phantom Radiotranslucent Ecg Monitoring Electrode (Jul 31, 1990)
- K893245: L30-LB- Infant Limb Band (Jun 20, 1989)
- K881085: Soft-E Series T-10 Accutrace Tab Resting Electrode (Apr 11, 1988)
- K871412: Contour Soft-E Series Conductive Solid Gel Electro (May 12, 1987)

Source page: https://510kreport.com/company/contour-electrodes