# Promatek Industries, Ltd.

- Location (FDA's records): Quebec, H4p 2c9, CA
- FDA decisions: 3 (1987–1990): 3 510(k) clearances
- Product codes: GZJ (1), IPF (1), LIH (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
- K901417: Electrostim MST (Aug 28, 1990)
- K873566: Electrostim I.F. (Feb 1, 1988)
- K871472: Kinestim Muscle Stimulator (Jun 29, 1987)

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