# Midwest Analog & Digital, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 3 (1978–1985): 3 510(k) clearances
- Product codes: DSF (1), DSI (1), DRT (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
- K850619: Bedside Patient Monitor W/Modules (Jun 6, 1985)
- K781873: Recorder, Strip Chart with Printer (Jan 5, 1979)
- K780432: Arrhythmia Program Module (May 26, 1978)

Source page: https://510kreport.com/company/midwest-analog-digital