# Midwest Development

- Location (FDA's records): Egale, WI
- FDA decisions: 1 (2005–2005): 1 510(k) clearance
- Product codes: IPF (1)
- Predicates its devices cite: 1 (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

## Firms whose devices it cites most
- Bio-Medical Research, Ltd.: 1 (https://510kreport.com/company/bio-medical-research)

## Recent decisions
- K050595: FT2000 Sequencer for  Muscle Stimulator (May 23, 2005)

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