# Ketronic, Inc.

- Location (FDA's records): The Netherlands, NL
- FDA decisions: 10 (1984–1985): 10 510(k) clearances
- Product codes: IYX (1), ISD (1), INO (1), BXB (1), ITI (1), ILK (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
- K850868: Mfe Cardiac Stress System (Jun 12, 1985)
- K850869: Mfe Couch Ergometer (Jun 12, 1985)
- K850873: Hilo Tables, Type CH-4, CH-8, FW-6, FW-5, FW-2, AL (Jun 12, 1985)
- K850877: Monolift MPE2, Platform, Chair, Fully Futo Platfor (Jun 12, 1985)
- K850870: Medifette Ergometer (Jun 12, 1985)
- K850872: Phyaction 300, 360, 370, 390 & 391 Elec-Muscle-Sti (Jun 6, 1985)
- K850871: Tredband Type I, IT, II & Iii - Treadmills (Jun 5, 1985)
- K850876: Ligtvoet L80.2 Lightfoot L80.2 Power Wheelchair (May 16, 1985)

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