# Surge Cardiovascular

- Location (FDA's records): Grand Rapids, MI
- FDA decisions: 1 (2017–2017): 1 510(k) clearance
- Product codes: DWF (1)
- Predicates its devices cite: 3 (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
- Chase Medical, Inc.: 1 (https://510kreport.com/company/chase-medical)
- Dlp, Inc.: 1 (https://510kreport.com/company/dlp)
- Sorin Group Italia S.R.L.: 1 (https://510kreport.com/company/sorin-group-italia)

## Recent decisions
- K170488: Peak Left Ventricular Vent Cannula, 20 Fr.; Peak Left Ventricular Vent Cannula, 18 Fr; Peak Left Ventricular Vent Cannula, 16 Fr (Aug 10, 2017)

Source page: https://510kreport.com/company/surge-cardiovascular