# Litton Datamedix

- Location (FDA's records): Mchenry, IL
- FDA decisions: 5 (1984–1986): 5 510(k) clearances
- Product codes: LDD (2), IYO (1), DXN (1), KLK (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
- K853599: Litton Datamedix Blood Pressure Monitor NI (Mar 21, 1986)
- K850290: Ultrasound Gel (Apr 18, 1985)
- K842497: Servomed Oxymonito SMK 363 (Oct 4, 1984)
- K842312: Servocard SCP-840 (Aug 27, 1984)
- K842235: Servocard Defibrillator SCP-851 (Aug 27, 1984)

Source page: https://510kreport.com/company/litton-datamedix