# G. Dundas Co.

- Location (FDA's records): Black Diamond, WA
- FDA decisions: 4 (1980–2011): 4 510(k) clearances
- Names in FDA's records: G. Dundas Co. (2); G. Dundas Co.,Inc. (2)
- Product codes: CBN (3), BSZ (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 3 (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
- Ohio Medical Products: 1 (https://510kreport.com/company/ohio-medical-products)
- Draeger Medical, Inc.: 1 (https://510kreport.com/company/draeger-medical)

## Firms that cite its devices most
- Parker Hannifin Corp.: 1 (https://510kreport.com/company/parker-hannifin)
- Sedation Systems, LLC: 1 (https://510kreport.com/company/sedation-systems)
- Linde Healthcare AB: 1 (https://510kreport.com/company/linde-healthcare)

## Its most-cited devices
- K080039: Passive Waste Gas Scavenger, Model 14600 (2008), cited by 2
- K110930: Active Waste Gas Scavenger (2011), cited by 1

## Recent decisions
- K110930: Active Waste Gas Scavenger (Jun 23, 2011)
- K080039: Passive Waste Gas Scavenger, Model 14600 (Apr 14, 2008)
- K963601: Model 1920 Waste Gas Scavenger (Apr 28, 1997)
- K802591: Model 5460 + 5480 Pop-Off Valves (Nov 12, 1980)

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