# Commwell, Ltd.

- Location (FDA's records): Washington, DC
- FDA decisions: 3 (2006–2011): 3 510(k) clearances
- Product codes: DPS (2), DRX (1)
- Predicates its devices cite: 3 (1 its own); citations of its devices by later devices: 2 (1 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
- Qrs Diagnostic, LLC: 1 (https://510kreport.com/company/qrs-diagnostic)
- Ge Medical Systems Information Technologies: 1 (https://510kreport.com/company/ge-medical-systems-information-technologies)

## Firms that cite its devices most
- Commwell R&D, Ltd.: 1 (https://510kreport.com/company/commwell-r-d)

## Its most-cited devices
- K050674: Physioglove ES (2006), cited by 1
- K103791: Physioglove ES with Ecg Analysis (2011), cited by 1

## Recent decisions
- K103791: Physioglove ES with Ecg Analysis (Oct 21, 2011)
- K083677: Physioglove for Use with Physioglove ES1 (Mar 10, 2009)
- K050674: Physioglove ES (Apr 25, 2006)

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