# Promedtek, Inc.

- Location (FDA's records): Washington, DC
- FDA decisions: 2 (2007–2016): 2 510(k) clearances
- Product codes: ILX (1), IMJ (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
- Mrt, Inc.: 1 (https://510kreport.com/company/mrt)
- Mettler Electronics Corp.: 1 (https://510kreport.com/company/mettler-electronics)

## Recent decisions
- K162240: ProMedTek Model C1400 Shortwave Diathermy Device (Nov 17, 2016)
- K070931: Model PMT850 (May 24, 2007)

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