# Avalon Laboratories, LLC

- Location (FDA's records): Rancho Dominguez, CA
- FDA decisions: 3 (2008–2008): 3 510(k) clearances
- Product codes: DWF (2), DRE (1)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 8 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Coombs Medical Device Consulting: 1 (https://510kreport.com/company/coombs-medical-device-consulting)
- Origen Biomedical, Inc.: 1 (https://510kreport.com/company/origen-biomedical)
- Medtronic Perfusion Systems: 1 (https://510kreport.com/company/medtronic-perfusion-systems)

## Firms that cite its devices most
- Cardiacassist, Inc.: 3 (https://510kreport.com/company/cardiacassist)
- Mc3 Incorporated: 2 (https://510kreport.com/company/mc3)
- Medtronic, Inc.: 1 (https://510kreport.com/company/medtronic)
- Maquet Cardiopulmonary, AG: 1 (https://510kreport.com/company/maquet-cardiopulmonary)
- Ultrasonix Medical Corpation: 1 (https://510kreport.com/company/ultrasonix-medical-corpation)

## Its most-cited devices
- K081820: Avalon Elite BI-Caval Dual Lumen Catheter, 13FR, 16FR, 19FR, 20FR, 23FR, 27FR, 31FR (2008), cited by 5
- K081940: Avalon Elite Vascular Access Kit (2008), cited by 3

## Recent decisions
- K081940: Avalon Elite Vascular Access Kit (Nov 18, 2008)
- K081820: Avalon Elite BI-Caval Dual Lumen Catheter, 13FR, 16FR, 19FR, 20FR, 23FR, 27FR, 31FR (Oct 6, 2008)
- K081933: Avalon Elite Multi-Port Venous Femoral Catheter, 20FR, 22FR, 24FR, 26FR, 28FR (Oct 3, 2008)

Source page: https://510kreport.com/company/avalon-laboratories