# Dymedso, Inc.

- Location (FDA's records): Springfield, VT
- FDA decisions: 3 (2007–2011): 3 510(k) clearances
- Product codes: BYI (3)
- Predicates its devices cite: 7 (2 its own); citations of its devices by later devices: 5 (2 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
- American Biosystems, Inc.: 1 (https://510kreport.com/company/american-biosystems)
- Bradstreet Clinical Research Assoc., Inc.: 1 (https://510kreport.com/company/bradstreet-clinical-research-assoc)
- Electromed, Inc.: 1 (https://510kreport.com/company/electromed)
- Advanced Respiratory: 1 (https://510kreport.com/company/advanced-respiratory)
- Med Systems: 1 (https://510kreport.com/company/med-systems)

## Firms that cite its devices most
- Westmed, Inc.: 3 (https://510kreport.com/company/westmed)

## Its most-cited devices
- K100749: Frequencer Model V2X (2010), cited by 2
- K063645: Frequencer, Model 1001 (2007), cited by 2
- K103176: Frequencer (2011), cited by 1

## Recent decisions
- K103176: Frequencer (Jan 26, 2011)
- K100749: Frequencer Model V2X (Aug 31, 2010)
- K063645: Frequencer, Model 1001 (Mar 15, 2007)

Source page: https://510kreport.com/company/dymedso