# Konica Medical and Graphic Corporation

- Location (FDA's records): Mie-Ken, JP
- FDA decisions: 1 (2003–2003): 1 510(k) clearance
- Product codes: LMC (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (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 that cite its devices most
- Konica Minolta Medical & Graphic, Inc.: 1 (https://510kreport.com/company/konica-minolta-medical-graphic)

## Its most-cited devices
- K032681: Konica Laser Imager, Model Drypro Model 771 (2003), cited by 1

## Recent decisions
- K032681: Konica Laser Imager, Model Drypro Model 771 (Sep 24, 2003)

Source page: https://510kreport.com/company/konica-medical-and-graphic