# Tokyo Boeki Medical System, Ltd.

- Location (FDA's records): Raleigh, NC
- FDA decisions: 1 (2005–2005): 1 510(k) clearance
- Product codes: JJE (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 2 (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
- Roche Diagnostic Systems, Inc.: 1 (https://510kreport.com/company/roche-diagnostic-systems)

## Firms that cite its devices most
- Tokyo Boeki Medisys, Inc.: 1 (https://510kreport.com/company/tokyo-boeki-medisys)
- Diamond Diagnostics, Inc.: 1 (https://510kreport.com/company/diamond-diagnostics)

## Its most-cited devices
- K040958: Prestige Models 24I and 400 and MGC Model 240 (2005), cited by 2

## Recent decisions
- K040958: Prestige Models 24I and 400 and MGC Model 240 (Feb 15, 2005)

Source page: https://510kreport.com/company/tokyo-boeki-medical-system