# Neuromusclar Electrical Stimulation Systems, Ltd.

- Location (FDA's records): Washington, DC
- FDA decisions: 2 (1996–2001): 2 510(k) clearances
- Product codes: IPF (1), GZI (1)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 6 (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
- Dynatronics Corp.: 1 (https://510kreport.com/company/dynatronics)
- Electro Med Supply, Inc.: 1 (https://510kreport.com/company/electro-med-supply)
- Medtronic Vascular: 1 (https://510kreport.com/company/medtronic-vascular)

## Firms that cite its devices most
- Ness-Neuromuscular Electrical Stimulation Systems: 5 (https://510kreport.com/company/ness-neuromuscular-electrical-stimulation-systems)
- N.E.S.S. Nuromuscular Electrical Stimulation Syst: 1 (https://510kreport.com/company/ness-nuromuscular-electrical-stimulation-syst)

## Its most-cited devices
- K952273: Handmaster NMS1 (1996), cited by 4
- K010837: Handmaster (2001), cited by 2

## Recent decisions
- K010837: Handmaster (Jun 15, 2001)
- K952273: Handmaster NMS1 (May 23, 1996)

Source page: https://510kreport.com/company/neuromusclar-electrical-stimulation-systems