# Amertek

- Location (FDA's records): Walker, MI
- FDA decisions: 2 (1981–1982): 2 510(k) clearances
- Product codes: DXN (1), DPS (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
- K821090: Cardi-O-Life Model 8823 (Jul 8, 1982)
- K812936: Blood Pressure Monitor (Dec 14, 1981)

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