# Kone Instruments, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 12 (1982–1987): 12 510(k) clearances
- Product codes: DRT (5), JJF (3), LDD (1), DRX (1), JFP (1), DSI (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
- K873345: 'Microlyte 4/5' (Sep 11, 1987)
- K870777: Progress Plus Selective Chemistry Analyzer (Mar 13, 1987)
- K863466: M700 Stress Monitor (Dec 22, 1986)
- K862655: Signa II Resting Ecg Electrode (Aug 6, 1986)
- K860767: Model E 600 Electrocardiograph (Apr 23, 1986)
- K853354: MEDIC 4 (Oct 11, 1985)
- K840200: Progress Selective Dhemistry Analyz (Apr 4, 1984)
- K830432: Central Station 590 (Mar 24, 1983)

Source page: https://510kreport.com/company/kone-instruments