# G & J Electronics, Inc.

- Location (FDA's records): Toronto, Ontario, CA
- FDA decisions: 2 (1999–1999): 2 510(k) clearances
- Product codes: FFX (2)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 5 (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
- Crospon, Ltd.: 3 (https://510kreport.com/company/crospon)
- Mui Scientific: 2 (https://510kreport.com/company/mui-scientific)

## Its most-cited devices
- K991288: Distender Series II Barostat (1999), cited by 4
- K973844: Gastric and Rectal Catheters (1999), cited by 1

## Recent decisions
- K991288: Distender Series II Barostat (Jun 8, 1999)
- K973844: Gastric and Rectal Catheters (Jun 4, 1999)

Source page: https://510kreport.com/company/g-j-electronics