# Honeywell, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 69 (1976–1990): 69 510(k) clearances
- Product codes: DPS (7), DRT (6), DSF (6), DXG (4), DSK (4), LDD (4), DXJ (4), DXK (3), DRJ (3), BZQ (3), DQC (2), IYO (2)
- 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
- K902230: Colorado Color Imaging Recorder (Jun 19, 1990)
- K863100: Cen Sta Mon AC/DC Alarm Central Acces Alarm Recor (Feb 3, 1987)
- K853501: Honeywell Electronic Ventilator EV-a (Apr 4, 1986)
- K855125: Physiological Telemetry Patient Monitoring System (Mar 26, 1986)
- K851888: Apm Dispos. Blood Pressure Transducer (Aug 6, 1985)
- K851496: Ecg Monitor Model RM102 (Jul 24, 1985)
- K850794: Patient Monitor Model RM-300 (Apr 18, 1985)
- K851092: Portable Defibrillator/Monitor ED 425 (Apr 10, 1985)

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