# Cross Vascular, Inc.

- Location (FDA's records): Solana Beach, CA
- FDA decisions: 2 (2023–2023): 2 510(k) clearances
- Product codes: DXF (1), GEI (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 2 (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
- Baylis Medical Co., Inc.: 2 (https://510kreport.com/company/baylis-medical)

## Firms that cite its devices most
- Atraverse Medical: 1 (https://510kreport.com/company/atraverse-medical)
- Circa Scientific, Inc.: 1 (https://510kreport.com/company/circa-scientific)

## Its most-cited devices
- K232852: Cross Vascular RF Transseptal Needle, Cross Vascular Connection Cable (2023), cited by 1
- K232809: Cross Vascular RF Generator and Footswitch (optional accessory) (2023), cited by 1

## Recent decisions
- K232852: Cross Vascular RF Transseptal Needle, Cross Vascular Connection Cable (Oct 12, 2023)
- K232809: Cross Vascular RF Generator and Footswitch (optional accessory) (Oct 12, 2023)

Source page: https://510kreport.com/company/cross-vascular