# Promatek

- Location (FDA's records): Canada   H4p 2c9, CA
- FDA decisions: 1 (1986–1986): 1 510(k) clearance
- Product codes: IPF (1)
- Predicates its devices cite: 0 (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

## Recent decisions
- K860619: ES 180-DCM Muscle Stimulator (May 30, 1986)

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