# Trudell Medical Int'L

- Location (FDA's records): London, CA
- FDA decisions: 3 (1999–2014): 3 510(k) clearances
- Product codes: CAF (3)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 4 (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
- Dhd Diemolding Healthcare Div.: 1 (https://510kreport.com/company/dhd-diemolding-healthcare-div)

## Firms that cite its devices most
- Respironics Healthscan, Inc.: 1 (https://510kreport.com/company/respironics-healthscan)
- Pari Innovative Manufacturers, Inc.: 1 (https://510kreport.com/company/pari-innovative-manufacturers)
- Activaero America, Inc.: 1 (https://510kreport.com/company/activaero-america)
- Respironics New Jersey, Inc.: 1 (https://510kreport.com/company/respironics-new-jersey)

## Its most-cited devices
- K992917: Aerochamber Plus Valved Holding Chamber (1999), cited by 4

## Recent decisions
- K140919: Respiconnect Adapter (Aug 15, 2014)
- K001137: Aerotrach Plus Valved Holding Chamber (VHC) (Jul 5, 2000)
- K992917: Aerochamber Plus Valved Holding Chamber (Sep 14, 1999)

Source page: https://510kreport.com/company/trudell-medical-int-l