# Medcraft Corp.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 5 (1976–1986): 5 510(k) clearances
- Product codes: DPS (2), DSH (1), QGH (1), IOL (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
- K860467: Electroshock Unit Neurology Model B-25 (Nov 10, 1986)
- K791795: Comp-Act IV (Sep 27, 1979)
- K760508: Accutape 24 (Aug 30, 1976)
- K760509: Treadmill, Diagnostic (Aug 30, 1976)
- K760510: Monitoring System, Rehabilitation (Aug 30, 1976)

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