# Eletromed, Inc.

- Location (FDA's records): Betheda, MD
- FDA decisions: 1 (2003–2003): 1 510(k) clearance
- Product codes: GXY (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 0 (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
- M & R Mfg., Inc.: 1 (https://510kreport.com/company/m-r-mfg)
- Pepin Mfg., Inc.: 1 (https://510kreport.com/company/pepin-mfg)

## Recent decisions
- K030800: Electromed Reusable Neurostimulation Electrodes (Jun 11, 2003)

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